A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974071



Internal ID18609284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27014640..27019568hg38UCSC Ensembl
Innerchr13:27588777..27593705hg19UCSC Ensembl
Innerchr13:26486777..26491705hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg384929
hg194929
hg184929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1957125, nssv1957124, nssv1957127, nssv1957131, nssv1957123, nssv1957129, nssv1957128, nssv1957130, nssv1957122, nssv1957126
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)nsv974071
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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