A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521905



Internal ID15449198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153691006..153698695hg38UCSC Ensembl
Innerchr3:153408795..153416484hg19UCSC Ensembl
Innerchr3:154891485..154899174hg18UCSC Ensembl
Innerchr3:154891493..154899182hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg387690
hg197690
hg187690
hg177690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694677
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521905
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