A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983063



Internal ID18271571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114407836..114408448hg38UCSC Ensembl
Innerchr11:114278558..114279170hg19UCSC Ensembl
Innerchr11:113783768..113784380hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38613
hg19613
hg18613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1902598, nssv1902602, nssv1902606, nssv1902599, nssv1902604, nssv1902603, nssv1902597, nssv1902601, nssv1902600, nssv1902605
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesRBM7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983063
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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