A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970867



Internal ID18606089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66428887..66435256hg38UCSC Ensembl
Innerchr7:65893874..65900243hg19UCSC Ensembl
Innerchr7:65531309..65537678hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg386370
hg196370
hg186370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2458803, nssv2458802, nssv2458806, nssv2458804, nssv2458811, nssv2458805, nssv2458809, nssv2458810, nssv2458807, nssv2458808
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)nsv970867
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