A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678962



Internal ID15068928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48514994..48515257hg38UCSC Ensembl
Innerchr10:49723037..49723300hg19UCSC Ensembl
Innerchr10:49393043..49393306hg18UCSC Ensembl
Innerchr10:49393043..49393306hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38264
hg19264
hg18264
hg17264
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516006
Supporting Variants
Samples
Known GenesARHGAP22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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