A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977257



Internal ID18612463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67891642..67916848hg38UCSC Ensembl
Innerchr13:68465774..68490980hg19UCSC Ensembl
Innerchr13:67363775..67388981hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3825207
hg1925207
hg1825207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1967579, nssv1967582, nssv1967577, nssv1967580, nssv1967576, nssv1967584, nssv1967583, nssv1967581, nssv1967575, nssv1967578
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)nsv977257
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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