A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983588



Internal ID18618781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52198326..52259403hg38UCSC Ensembl
Innerchr13:52772461..52833538hg19UCSC Ensembl
Innerchr13:51670462..51731539hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3861078
hg1961078
hg1861078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1964563, nssv1964564, nssv1964565, nssv1964559, nssv1964562, nssv1964566, nssv1964557, nssv1964561, nssv1964560, nssv1964558
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)nsv983588
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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