A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967080



Internal ID18602309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156712531..156715059hg38UCSC Ensembl
Innerchr3:156430320..156432848hg19UCSC Ensembl
Innerchr3:157913014..157915542hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg382529
hg192529
hg182529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2301923, nssv2301914, nssv2301920, nssv2301919, nssv2301922, nssv2301921, nssv2301915, nssv2301917, nssv2301916, nssv2301918
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)nsv967080
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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