A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173556



Internal ID15508412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43199601..43304140hg38UCSC Ensembl
Innerchr10:43695049..43799588hg19UCSC Ensembl
Innerchr10:43015055..43119594hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38104540
hg19104540
hg18104540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550696
Supporting Variants
Samples1780862444_A
Known GenesRASGEF1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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