A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969342



Internal ID18604569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:310300..320019hg38UCSC Ensembl
Innerchr6:310300..320019hg19UCSC Ensembl
Innerchr6:255300..265019hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg389720
hg199720
hg189720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2391762, nssv2391768, nssv2391765, nssv2391766, nssv2391759, nssv2391764, nssv2391767, nssv2391760, nssv2391763, nssv2391761
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDUSP22
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969342
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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