A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977697



Internal ID18266217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34793028..34793618hg38UCSC Ensembl
Innerchr15:35085229..35085819hg19UCSC Ensembl
Innerchr15:32872521..32873111hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38591
hg19591
hg18591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2017625, nssv2017622, nssv2017623, nssv2017627, nssv2017619, nssv2017621, nssv2017626, nssv2017620, nssv2017628, nssv2017624
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesACTC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977697
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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