A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963734



Internal ID18252288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:151576961..151609743hg38UCSC Ensembl
Innerchr2:152433475..152466257hg19UCSC Ensembl
Innerchr2:152141721..152174503hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3832783
hg1932783
hg1832783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2207794, nssv2207787, nssv2207795, nssv2207789, nssv2207791, nssv2207788, nssv2207793, nssv2207792, nssv2207786, nssv2207790
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNEB
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963734
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