A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523722



Internal ID15451015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11642043..11694957hg38UCSC Ensembl
Innerchr10:11684042..11736956hg19UCSC Ensembl
Innerchr10:11724048..11776962hg18UCSC Ensembl
Innerchr10:11724048..11776962hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852915
hg1952915
hg1852915
hg1752915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699537
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523722
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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