A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976074



Internal ID18264595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18638167..18927720hg38UCSC Ensembl
Innerchr13:19212307..19501860hg19UCSC Ensembl
Innerchr13:18110307..18399860hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38289554
hg19289554
hg18289554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1950430, nssv1950427, nssv1950428, nssv1950431, nssv1950432, nssv1950426, nssv1950433, nssv1950434, nssv1950429, nssv1950425
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANKRD20A9P, LINC00408, LINC00417
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976074
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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