A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687387



Internal ID15077353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16019962..16043720hg38UCSC Ensembl
Innerchr1:16346457..16370215hg19UCSC Ensembl
Innerchr1:16219044..16242802hg18UCSC Ensembl
Innerchr1:16091763..16115521hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3823759
hg1923759
hg1823759
hg1723759
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517651
Supporting Variants
Samples
Known GenesCLCNKA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687387
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