A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965713



Internal ID18600943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34740411..34746074hg38UCSC Ensembl
Innerchr6:34708188..34713851hg19UCSC Ensembl
Innerchr6:34816166..34821829hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385664
hg195664
hg185664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2404369, nssv2404901, nssv2404371, nssv2404368, nssv2404370, nssv2404365, nssv2404366, nssv2404364, nssv2404900, nssv2404367
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)nsv965713
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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