A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969414



Internal ID18604641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61109123..61166777hg38UCSC Ensembl
Innerchr6:62070937..62128589hg19UCSC Ensembl
Innerchr6:62128896..62186716hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3857655
hg1957653
hg1857821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2411152, nssv2411153, nssv2411154, nssv2411156, nssv2411155, nssv2411151, nssv2411150, nssv2411149, nssv2411157, nssv2411158
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)nsv969414
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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