A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969359



Internal ID18604586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26443433..26453013hg38UCSC Ensembl
Innerchr6:26443661..26453241hg19UCSC Ensembl
Innerchr6:26551640..26561220hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg389581
hg199581
hg189581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2397776, nssv2397778, nssv2397781, nssv2397785, nssv2397784, nssv2397777, nssv2397782, nssv2397779, nssv2397783, nssv2397780
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBTN3A3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969359
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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