A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963762



Internal ID18599002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:202611974..202614869hg38UCSC Ensembl
Innerchr2:203476697..203479592hg19UCSC Ensembl
Innerchr2:203184942..203187837hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg382896
hg192896
hg182896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2672708, nssv2672701, nssv2672714, nssv2672705, nssv2672709, nssv2672716, nssv2672719, nssv2672711, nssv2672717, nssv2672706, nssv2672703, nssv2672710, nssv2672700, nssv2672712, nssv2672718, nssv2672702, nssv2672715, nssv2672707, nssv2672713, nssv2672704
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963762
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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