A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671887



Internal ID15408539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75113848..75131338hg38UCSC Ensembl
Innerchr10:76873606..76891096hg19UCSC Ensembl
Innerchr10:76543612..76561102hg18UCSC Ensembl
Innerchr10:76543612..76561102hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3817491
hg1917491
hg1817491
hg1717491
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520500
Supporting Variants
Samples
Known GenesSAMD8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671887
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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