A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964077



Internal ID18599315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98740858..98742419hg38UCSC Ensembl
Innerchr4:99662009..99663570hg19UCSC Ensembl
Innerchr4:99881032..99882593hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381562
hg191562
hg181562
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2326796, nssv2326792, nssv2326794, nssv2326797, nssv2326795, nssv2326789, nssv2326793, nssv2326791, nssv2326798, nssv2326790
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)nsv964077
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