A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981182



Internal ID18616381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121857322..121860570hg38UCSC Ensembl
Innerchr6:122178468..122181716hg19UCSC Ensembl
Innerchr6:122220167..122223415hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383249
hg193249
hg183249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2421616, nssv2421612, nssv2421614, nssv2421610, nssv2421611, nssv2421615, nssv2421609, nssv2421617, nssv2421608, nssv2421613
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)nsv981182
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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