A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965728



Internal ID18600958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:56869090..56875835hg38UCSC Ensembl
Innerchr6:56733888..56740633hg19UCSC Ensembl
Innerchr6:56841847..56848592hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg386746
hg196746
hg186746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2410655, nssv2408024, nssv2410656, nssv2408026, nssv2408027, nssv2408025, nssv2410653, nssv2408029, nssv2410654, nssv2408028
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDST
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965728
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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