A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970189



Internal ID18605413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160751995..160754058hg38UCSC Ensembl
Innerchr6:161173027..161175090hg19UCSC Ensembl
Innerchr6:161093017..161095080hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382064
hg192064
hg182064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429851, nssv2429854, nssv2429849, nssv2429856, nssv2429848, nssv2429852, nssv2429850, nssv2429853, nssv2429855, nssv2429857
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPLG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970189
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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