A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516700



Internal ID15097307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15632006..15632136hg38UCSC Ensembl
Innerchr10:15674005..15674135hg19UCSC Ensembl
Innerchr10:15714011..15714141hg18UCSC Ensembl
Innerchr10:15714011..15714141hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38131
hg19131
hg18131
hg17131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691009, nssv670223, nssv687436
Samples
Known GenesITGA8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516700
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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