A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520941



Internal ID15448234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5861555..5862955hg38UCSC Ensembl
Innerchr10:5903518..5904918hg19UCSC Ensembl
Innerchr10:5943524..5944924hg18UCSC Ensembl
Innerchr10:5943524..5944924hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381401
hg191401
hg181401
hg171401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697699
Samples
Known GenesANKRD16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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