A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677422



Internal ID15414074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57959868..57977219hg38UCSC Ensembl
Innerchr13:58534002..58551353hg19UCSC Ensembl
Innerchr13:57432003..57449354hg18UCSC Ensembl
Innerchr13:57432003..57449354hg17UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3817352
hg1917352
hg1817352
hg1717352
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517500
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677422
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