A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516006



Internal ID15096613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48499899..48515257hg38UCSC Ensembl
Innerchr10:49707942..49723300hg19UCSC Ensembl
Innerchr10:49377948..49393306hg18UCSC Ensembl
Innerchr10:49377948..49393306hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815359
hg1915359
hg1815359
hg1715359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688239, nssv678962, nssv669185, nssv658140, nssv669087, nssv665684
Samples
Known GenesARHGAP22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516006
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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