A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517636



Internal ID15444929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113159689..113174793hg38UCSC Ensembl
Innerchr3:112878536..112893640hg19UCSC Ensembl
Innerchr3:114361226..114376330hg18UCSC Ensembl
Innerchr3:114361226..114376330hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3815105
hg1915105
hg1815105
hg1715105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652632, nssv699604, nssv689859
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517636
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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