A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965744



Internal ID18600974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:87442004..87444950hg38UCSC Ensembl
Innerchr6:88151722..88154668hg19UCSC Ensembl
Innerchr6:88208441..88211387hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382947
hg192947
hg182947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2417192, nssv2417190, nssv2417188, nssv2417191, nssv2417194, nssv2417189, nssv2417195, nssv2417197, nssv2417196, nssv2417193
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC6orf165
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965744
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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