A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981154



Internal ID18616353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63544045..63550204hg38UCSC Ensembl
Innerchr6:64253950..64260109hg19UCSC Ensembl
Innerchr6:64311909..64318068hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386160
hg196160
hg186160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2414201, nssv2414197, nssv2414196, nssv2414202, nssv2414203, nssv2414199, nssv2414200, nssv2414195, nssv2414204, nssv2414198
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)nsv981154
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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