A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963366



Internal ID18598607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150051291..150052153hg38UCSC Ensembl
Innerchr3:149769078..149769940hg19UCSC Ensembl
Innerchr3:151251768..151252630hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38863
hg19863
hg18863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2301468, nssv2301459, nssv2301464, nssv2301461, nssv2301463, nssv2301462, nssv2301460, nssv2301465, nssv2301466, nssv2301467
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)nsv963366
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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