A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970136



Internal ID18605360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65836872..65837970hg38UCSC Ensembl
Innerchr6:66546765..66547863hg19UCSC Ensembl
Innerchr6:66603486..66604584hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2413849, nssv2413848, nssv2413847, nssv2413845, nssv2413852, nssv2413846, nssv2413850, nssv2413854, nssv2413851, nssv2413853
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)nsv970136
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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