A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519773



Internal ID15447066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5862337..5863268hg38UCSC Ensembl
Innerchr10:5904300..5905231hg19UCSC Ensembl
Innerchr10:5944306..5945237hg18UCSC Ensembl
Innerchr10:5944306..5945237hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38932
hg19932
hg18932
hg17932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685026, nssv660681, nssv684268, nssv658449, nssv686097
Samples
Known GenesANKRD16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519773
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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