A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975197



Internal ID18263719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66676345..66678236hg38UCSC Ensembl
Innerchr11:66443816..66445707hg19UCSC Ensembl
Innerchr11:66200392..66202283hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381892
hg191892
hg181892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1893665, nssv1893671, nssv1893670, nssv1893667, nssv1893668, nssv1893674, nssv1893666, nssv1893673, nssv1893669, nssv1893672
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRBM4B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975197
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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