A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963368



Internal ID18598609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152917868..152921468hg38UCSC Ensembl
Innerchr3:152635657..152639257hg19UCSC Ensembl
Innerchr3:154118347..154121947hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg383601
hg193601
hg183601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2299934, nssv2299932, nssv2299925, nssv2299931, nssv2299927, nssv2299928, nssv2299930, nssv2299933, nssv2299926, nssv2299929
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)nsv963368
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