A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661132



Internal ID15397784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120976908..121004668hg38UCSC Ensembl
Innerchr10:122736421..122764181hg19UCSC Ensembl
Innerchr10:122726411..122754171hg18UCSC Ensembl
Innerchr10:122726411..122754171hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3827761
hg1927761
hg1827761
hg1727761
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516037
Supporting Variants
Samples
Known GenesMIR5694
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661132
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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