A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436924



Internal ID15035740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10646034..10657540hg38UCSC Ensembl
Outerchr1:10644631..10672212hg38UCSC Ensembl
Innerchr1:10706091..10717597hg19UCSC Ensembl
Outerchr1:10704688..10732269hg19UCSC Ensembl
Innerchr1:10628678..10640184hg18UCSC Ensembl
Outerchr1:10627275..10654856hg18UCSC Ensembl
Innerchr1:10415637..10427143hg16UCSC Ensembl
Outerchr1:10414234..10441815hg16UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3827582
hg1927582
hg1827582
hg1627582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466805
SamplesNA10847
Known GenesCASZ1
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)nsv436924
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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