A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974073



Internal ID18609286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28536167..28539646hg38UCSC Ensembl
Innerchr13:29110304..29113783hg19UCSC Ensembl
Innerchr13:28008304..28011783hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg383480
hg193480
hg183480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1957906, nssv1957909, nssv1957911, nssv1957910, nssv1957914, nssv1957908, nssv1957912, nssv1957915, nssv1957913, nssv1957907
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)nsv974073
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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