A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969432



Internal ID18604659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100889774..100891794hg38UCSC Ensembl
Innerchr6:101337650..101339670hg19UCSC Ensembl
Innerchr6:101444371..101446391hg18UCSC Ensembl
Cytoband6q16.3
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 Variantsnssv2418739, nssv2418744, nssv2418740, nssv2418736, nssv2418737, nssv2418741, nssv2418735, nssv2418742, nssv2418738, nssv2418743
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)nsv969432
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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