A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699212



Internal ID15435864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63957408..63959993hg38UCSC Ensembl
Innerchr13:64531541..64534126hg19UCSC Ensembl
Innerchr13:63429542..63432127hg18UCSC Ensembl
Innerchr13:63429542..63432127hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg382586
hg192586
hg182586
hg172586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699212
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