A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969463



Internal ID18258004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160493093..160497203hg38UCSC Ensembl
Innerchr6:160914125..160918235hg19UCSC Ensembl
Innerchr6:160834115..160838225hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384111
hg194111
hg184111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429081, nssv2429080, nssv2429075, nssv2429078, nssv2429076, nssv2429077, nssv2429072, nssv2429079, nssv2429074, nssv2429073
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLPAL2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969463
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