A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960645



Internal ID18595892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2943619..2946809hg38UCSC Ensembl
Innerchr18:2943617..2946807hg19UCSC Ensembl
Innerchr18:2933617..2936807hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383191
hg193191
hg183191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2112303, nssv2112296, nssv2112297, nssv2112299, nssv2112295, nssv2112302, nssv2112301, nssv2112304, nssv2112298, nssv2112300
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC727896, LPIN2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960645
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