A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437127



Internal ID15035859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89184902..89186051hg38UCSC Ensembl
Outerchr10:89180246..89208346hg38UCSC Ensembl
Innerchr10:90944659..90945808hg19UCSC Ensembl
Outerchr10:90940003..90968103hg19UCSC Ensembl
Innerchr10:90934639..90935788hg18UCSC Ensembl
Outerchr10:90929983..90958083hg18UCSC Ensembl
Innerchr10:90609236..90610385hg16UCSC Ensembl
Outerchr10:90604580..90632680hg16UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3828101
hg1928101
hg1828101
hg1628101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467008
SamplesNA07048
Known GenesCH25H
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437127
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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