A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522179



Internal ID15102786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95235850..95240102hg38UCSC Ensembl
Innerchr13:95888104..95892356hg19UCSC Ensembl
Innerchr13:94686105..94690357hg18UCSC Ensembl
Innerchr13:94686105..94690357hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg384253
hg194253
hg184253
hg174253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694952
Samples
Known GenesABCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522179
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