A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705683



Internal ID15095649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133492654..133519299hg38UCSC Ensembl
Innerchr10:135306158..135332803hg19UCSC Ensembl
Innerchr10:135156148..135182793hg18UCSC Ensembl
Innerchr10:135195039..135221684hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3826646
hg1926646
hg1826646
hg1726646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517180
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705683
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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