A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675599



Internal ID15065565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98436902..98450195hg38UCSC Ensembl
Innerchr13:99089156..99102449hg19UCSC Ensembl
Innerchr13:97887157..97900450hg18UCSC Ensembl
Innerchr13:97887157..97900450hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3813294
hg1913294
hg1813294
hg1713294
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517409
Supporting Variants
Samples
Known GenesFARP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675599
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