A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970165



Internal ID18605389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132272113..132273113hg38UCSC Ensembl
Innerchr6:132593252..132594252hg19UCSC Ensembl
Innerchr6:132634945..132635945hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2424057, nssv2424055, nssv2424056, nssv2424061, nssv2424059, nssv2424053, nssv2424054, nssv2424052, nssv2424060, nssv2424058
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)nsv970165
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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