A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977220



Internal ID18612426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27696122..27707713hg38UCSC Ensembl
Innerchr13:28270259..28281850hg19UCSC Ensembl
Innerchr13:27168259..27179850hg18UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3811592
hg1911592
hg1811592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1956732, nssv1956729, nssv1956726, nssv1956735, nssv1956731, nssv1956733, nssv1956734, nssv1956727, nssv1956730, nssv1956728
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)nsv977220
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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