A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516870



Internal ID15097477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117945927..118028672hg38UCSC Ensembl
Innerchr10:119705438..119788183hg19UCSC Ensembl
Innerchr10:119695428..119778173hg18UCSC Ensembl
Innerchr10:119695428..119778173hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3882746
hg1982746
hg1882746
hg1782746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685789, nssv654601
Samples
Known GenesRAB11FIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516870
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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