A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976097



Internal ID18611304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25162551..25165677hg38UCSC Ensembl
Innerchr13:25736689..25739815hg19UCSC Ensembl
Innerchr13:24634689..24637815hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg383127
hg193127
hg183127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1955609, nssv1955611, nssv1955605, nssv1955612, nssv1955613, nssv1955608, nssv1955606, nssv1955614, nssv1955610, nssv1955607
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976097
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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