A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945773



Internal ID18592624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12136131..12137441hg38UCSC Ensembl
Innerchr1:12196188..12197498hg19UCSC Ensembl
Innerchr1:12118775..12120085hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381311
hg191311
hg181311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1753176, nssv1753175, nssv1753183, nssv1753180, nssv1753177, nssv1753179, nssv1754108, nssv1753178, nssv1753182, nssv1753181
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTNFRSF8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945773
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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