A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981201



Internal ID18616400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159748492..159750866hg38UCSC Ensembl
Innerchr6:160169524..160171898hg19UCSC Ensembl
Innerchr6:160089514..160091888hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382375
hg192375
hg182375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429195, nssv2429199, nssv2429196, nssv2429194, nssv2429200, nssv2429197, nssv2429192, nssv2429193, nssv2429198, nssv2429191
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWTAP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981201
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer