A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692375



Internal ID15082341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70697441..70737376hg38UCSC Ensembl
Innerchr16:70731344..70771279hg19UCSC Ensembl
Innerchr16:69288845..69328780hg18UCSC Ensembl
Innerchr16:69288845..69328780hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3839936
hg1939936
hg1839936
hg1739936
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesVAC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692375
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