A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963369



Internal ID18598610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153066338..153068421hg38UCSC Ensembl
Innerchr3:152784127..152786210hg19UCSC Ensembl
Innerchr3:154266817..154268900hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382084
hg192084
hg182084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2300028, nssv2300029, nssv2300022, nssv2300030, nssv2300024, nssv2300025, nssv2300026, nssv2300031, nssv2300023, nssv2300027
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963369
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