A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981446



Internal ID18616643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32812028..32862733hg38UCSC Ensembl
Innerchr7:32851640..32902345hg19UCSC Ensembl
Innerchr7:32818165..32868870hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3850706
hg1950706
hg1850706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2441596, nssv2441595, nssv2441591, nssv2441598, nssv2441597, nssv2441592, nssv2441599, nssv2441594, nssv2441593, nssv2441590
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)nsv981446
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