A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970157



Internal ID18605381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106641699..106643089hg38UCSC Ensembl
Innerchr6:107089574..107090964hg19UCSC Ensembl
Innerchr6:107196267..107197657hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381391
hg191391
hg181391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2419033, nssv2419036, nssv2419028, nssv2419027, nssv2419029, nssv2419034, nssv2419032, nssv2419030, nssv2419035, nssv2419031
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesQRSL1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970157
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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