A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683138



Internal ID15419790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010971..121024758hg38UCSC Ensembl
Innerchr10:122770484..122784271hg19UCSC Ensembl
Innerchr10:122760474..122774261hg18UCSC Ensembl
Innerchr10:122760474..122774261hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3813788
hg1913788
hg1813788
hg1713788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516918
Supporting Variants
Samples
Known GenesMIR5694
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683138
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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