A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965678



Internal ID18600908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7336326..7340815hg38UCSC Ensembl
Innerchr6:7336559..7341048hg19UCSC Ensembl
Innerchr6:7281558..7286047hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384490
hg194490
hg184490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393981, nssv2393983, nssv2393986, nssv2393985, nssv2393989, nssv2393988, nssv2393990, nssv2393984, nssv2393982, nssv2393987
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCAGE1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965678
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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