A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660178



Internal ID15396830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81112070..81123719hg38UCSC Ensembl
Innerchr16:81145675..81157324hg19UCSC Ensembl
Innerchr16:79703176..79714825hg18UCSC Ensembl
Innerchr16:79703176..79714825hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3811650
hg1911650
hg1811650
hg1711650
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520035
Supporting Variants
Samples
Known GenesPKD1L2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660178
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