A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963305



Internal ID18598546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27633538..27635805hg38UCSC Ensembl
Innerchr3:27675029..27677296hg19UCSC Ensembl
Innerchr3:27650033..27652300hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382268
hg192268
hg182268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2275550, nssv2275545, nssv2275548, nssv2275552, nssv2275549, nssv2275554, nssv2275547, nssv2275553, nssv2275546, nssv2275551
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963305
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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