A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696328



Internal ID15086294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75505987..75529848hg38UCSC Ensembl
Innerchr16:75539885..75563746hg19UCSC Ensembl
Innerchr16:74097386..74121247hg18UCSC Ensembl
Innerchr16:74097386..74121247hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3823862
hg1923862
hg1823862
hg1723862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516675
Supporting Variants
Samples
Known GenesCHST5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696328
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