A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981136



Internal ID18616335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37044957..37046009hg38UCSC Ensembl
Innerchr6:37012733..37013785hg19UCSC Ensembl
Innerchr6:37120711..37121763hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg381053
hg191053
hg181053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2407517, nssv2407511, nssv2407510, nssv2407513, nssv2407509, nssv2407512, nssv2407508, nssv2407514, nssv2407516, nssv2407515
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)nsv981136
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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