A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981180



Internal ID18616379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121407571..121410707hg38UCSC Ensembl
Innerchr6:121728717..121731853hg19UCSC Ensembl
Innerchr6:121770416..121773552hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383137
hg193137
hg183137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2422263, nssv2422268, nssv2422266, nssv2422260, nssv2422261, nssv2422264, nssv2422265, nssv2422269, nssv2422262, nssv2422267
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)nsv981180
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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