A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665856



Internal ID15402508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120976908..121001029hg38UCSC Ensembl
Innerchr10:122736421..122760542hg19UCSC Ensembl
Innerchr10:122726411..122750532hg18UCSC Ensembl
Innerchr10:122726411..122750532hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3824122
hg1924122
hg1824122
hg1724122
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)nssv665856
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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