A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2690908



Internal ID17772324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15143996..15146636hg38UCSC Ensembl
Innerchr3:15185503..15188143hg19UCSC Ensembl
Innerchr3:15160507..15163147hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382641
hg192641
hg182641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963402
Supporting Variants
SamplesHGDP00542
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2690908
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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