A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040924



Internal ID19130143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4691984..4723414hg38UCSC Ensembl
Innerchr10:4734176..4765606hg19UCSC Ensembl
Innerchr10:4724176..4755606hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3831431
hg1931431
hg1831431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707670
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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