A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699604



Internal ID15436256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113159689..113160864hg38UCSC Ensembl
Innerchr3:112878536..112879711hg19UCSC Ensembl
Innerchr3:114361226..114362401hg18UCSC Ensembl
Innerchr3:114361226..114362401hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg381176
hg191176
hg181176
hg171176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517636
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699604
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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