A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695605



Internal ID15432257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57770006..57786228hg38UCSC Ensembl
Innerchr19:58281374..58297596hg19UCSC Ensembl
Innerchr19:62973186..62989408hg18UCSC Ensembl
Innerchr19:62973186..62989408hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3816223
hg1916223
hg1816223
hg1716223
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520155
Supporting Variants
Samples
Known GenesZNF586
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695605
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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