A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972077



Internal ID18260607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118559802..118564878hg38UCSC Ensembl
Innerchr11:118430517..118435593hg19UCSC Ensembl
Innerchr11:117935727..117940803hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385077
hg195077
hg185077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1905982, nssv1905987, nssv1905989, nssv1905985, nssv1905980, nssv1905986, nssv1905983, nssv1905981, nssv1905984, nssv1905988
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesIFT46
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972077
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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