A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695636



Internal ID15085602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76509101..76512491hg38UCSC Ensembl
Innerchr10:78268859..78272249hg19UCSC Ensembl
Innerchr10:77938865..77942255hg18UCSC Ensembl
Innerchr10:77938865..77942255hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383391
hg193391
hg183391
hg173391
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518212
Supporting Variants
Samples
Known GenesC10orf11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695636
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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