A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523529



Internal ID15450822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143496630..143510727hg38UCSC Ensembl
Innerchr3:143215472..143229569hg19UCSC Ensembl
Innerchr3:144698162..144712259hg18UCSC Ensembl
Innerchr3:144698170..144712267hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3814098
hg1914098
hg1814098
hg1714098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699303
Samples
Known GenesSLC9A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523529
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