A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961911



Internal ID18597157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174780558..174781241hg38UCSC Ensembl
Innerchr2:175645286..175645969hg19UCSC Ensembl
Innerchr2:175353532..175354215hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38684
hg19684
hg18684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2211746, nssv2211739, nssv2211744, nssv2211742, nssv2211745, nssv2211743, nssv2211737, nssv2211738, nssv2211741, nssv2211740
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961911
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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