A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975979



Internal ID18264500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112088953..112096507hg38UCSC Ensembl
Innerchr11:111959677..111967231hg19UCSC Ensembl
Innerchr11:111464887..111472441hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387555
hg197555
hg187555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904603, nssv1904600, nssv1904602, nssv1904604, nssv1904597, nssv1904605, nssv1904599, nssv1904598, nssv1904606, nssv1904601
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSDHD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975979
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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