A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963211



Internal ID18598452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11075431..11077851hg38UCSC Ensembl
Innerchr2:11215557..11217977hg19UCSC Ensembl
Innerchr2:11133008..11135428hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382421
hg192421
hg182421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2163887, nssv2163884, nssv2163890, nssv2163888, nssv2163883, nssv2163886, nssv2163885, nssv2163891, nssv2163882, nssv2163889
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)nsv963211
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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