A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961017



Internal ID18596264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11424659..11425255hg38UCSC Ensembl
Innerchr2:11564785..11565381hg19UCSC Ensembl
Innerchr2:11482236..11482832hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38597
hg19597
hg18597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2162711, nssv2162710, nssv2162709, nssv2162703, nssv2162705, nssv2162708, nssv2162704, nssv2162707, nssv2162712, nssv2162706
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)nsv961017
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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