A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701557



Internal ID15091523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124606396..124607102hg38UCSC Ensembl
Innerchr10:126294965..126295671hg19UCSC Ensembl
Innerchr10:126284955..126285661hg18UCSC Ensembl
Innerchr10:126284955..126285661hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38707
hg19707
hg18707
hg17707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521161
Supporting Variants
Samples
Known GenesLHPP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701557
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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