A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981458



Internal ID18616655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39852843..39853681hg38UCSC Ensembl
Innerchr7:39892442..39893280hg19UCSC Ensembl
Innerchr7:39858967..39859805hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38839
hg19839
hg18839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2444548, nssv2444546, nssv2444549, nssv2444545, nssv2444543, nssv2444542, nssv2444540, nssv2444544, nssv2444541, nssv2444547
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)nsv981458
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