A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520125



Internal ID15447418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143302028..143310180hg38UCSC Ensembl
Innerchr3:143020870..143029022hg19UCSC Ensembl
Innerchr3:144503560..144511712hg18UCSC Ensembl
Innerchr3:144503568..144511720hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg388153
hg198153
hg188153
hg178153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697236
Samples
Known GenesSLC9A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520125
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