A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970800



Internal ID18606022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21400938..21407119hg38UCSC Ensembl
Innerchr7:21440556..21446737hg19UCSC Ensembl
Innerchr7:21407081..21413262hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386182
hg196182
hg186182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2437297, nssv2437292, nssv2437293, nssv2437294, nssv2437295, nssv2437296, nssv2437300, nssv2437299, nssv2437298, nssv2437301
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)nsv970800
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