A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975952



Internal ID18611159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77812520..77814983hg38UCSC Ensembl
Innerchr11:77523566..77526029hg19UCSC Ensembl
Innerchr11:77201214..77203677hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382464
hg192464
hg182464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1896430, nssv1896436, nssv1896435, nssv1896434, nssv1896431, nssv1896439, nssv1896433, nssv1896438, nssv1896437, nssv1896432
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRSF1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975952
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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