A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437055



Internal ID15035729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15402848..15803049hg38UCSC Ensembl
Outerchr8:15398926..15806828hg38UCSC Ensembl
Innerchr8:15260357..15660558hg19UCSC Ensembl
Outerchr8:15256435..15664337hg19UCSC Ensembl
Innerchr8:15304728..15704929hg18UCSC Ensembl
Outerchr8:15300806..15708708hg18UCSC Ensembl
Innerchr8:15270723..15670924hg16UCSC Ensembl
Outerchr8:15266801..15674703hg16UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38407903
hg19407903
hg18407903
hg16407903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466936
SamplesNA10863
Known GenesTUSC3
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)nsv437055
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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