A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981097



Internal ID18616296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:349825..354614hg38UCSC Ensembl
Innerchr6:349825..354614hg19UCSC Ensembl
Innerchr6:294825..299614hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg384790
hg194790
hg184790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2391784, nssv2391789, nssv2391787, nssv2391786, nssv2391788, nssv2391783, nssv2391785, nssv2391782, nssv2391781, nssv2391790
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)nsv981097
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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