A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969385



Internal ID18604612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32876751..32883068hg38UCSC Ensembl
Innerchr6:32844528..32850845hg19UCSC Ensembl
Innerchr6:32952506..32958823hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386318
hg196318
hg186318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2404762, nssv2404764, nssv2404765, nssv2404770, nssv2404766, nssv2404769, nssv2404763, nssv2404768, nssv2404761, nssv2404767
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)nsv969385
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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