A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976147



Internal ID18611354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95618818..95619887hg38UCSC Ensembl
Innerchr13:96271072..96272141hg19UCSC Ensembl
Innerchr13:95069073..95070142hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381070
hg191070
hg181070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1972114, nssv1972109, nssv1972113, nssv1972108, nssv1972110, nssv1972107, nssv1972115, nssv1972111, nssv1972112, nssv1972116
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDZIP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976147
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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