A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972038



Internal ID18607254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65144081..65145952hg38UCSC Ensembl
Innerchr11:64911552..64913423hg19UCSC Ensembl
Innerchr11:64668128..64669999hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381872
hg191872
hg181872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1893070, nssv1893072, nssv1893075, nssv1893069, nssv1893076, nssv1893074, nssv1893077, nssv1893073, nssv1893068, nssv1893071
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)nsv972038
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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