A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967081



Internal ID18602310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156809501..156811521hg38UCSC Ensembl
Innerchr3:156527290..156529310hg19UCSC Ensembl
Innerchr3:158009984..158012004hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg382021
hg192021
hg182021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2302543, nssv2302540, nssv2302547, nssv2302541, nssv2302542, nssv2302546, nssv2302539, nssv2302548, nssv2302545, nssv2302544
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00886, PA2G4P4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967081
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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