A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700065



Internal ID15436717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23559556..24307497hg38UCSC Ensembl
Innerchr19:23742358..24490299hg19UCSC Ensembl
Innerchr19:23534198..24282139hg18UCSC Ensembl
Innerchr19:23534198..24282139hg17UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38747942
hg19747942
hg18747942
hg17747942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524183
Supporting Variants
Samples
Known GenesHAVCR1P1, RPSAP58, ZNF254, ZNF675, ZNF681, ZNF726
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700065
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer