A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695690



Internal ID15432342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:38074651..38087756hg38UCSC Ensembl
Innerchr13:38648788..38661893hg19UCSC Ensembl
Innerchr13:37546788..37559893hg18UCSC Ensembl
Innerchr13:37546788..37559893hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3813106
hg1913106
hg1813106
hg1713106
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518259
Supporting Variants
Samples
Known GenesLINC00571
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695690
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