A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970111



Internal ID18605335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41306585..41308911hg38UCSC Ensembl
Innerchr6:41274323..41276649hg19UCSC Ensembl
Innerchr6:41382301..41384627hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382327
hg192327
hg182327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2408608, nssv2408614, nssv2408610, nssv2408617, nssv2408611, nssv2408613, nssv2408609, nssv2408615, nssv2408612, nssv2408616
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)nsv970111
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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