A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516037



Internal ID15443094
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671440, nssv665856, nssv667613, nssv661132, nssv654984, nssv657652
Samples
Known GenesMIR5694
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516037
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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