A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704679



Internal ID15094645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:61643477..61716352hg38UCSC Ensembl
Innerchr10:63403235..63476110hg19UCSC Ensembl
Innerchr10:63073241..63146116hg18UCSC Ensembl
Innerchr10:63073241..63146116hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3872876
hg1972876
hg1872876
hg1772876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528134
Supporting Variants
Samples
Known GenesC10orf107
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704679
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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