A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997534



Internal ID18810384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3934721..4221511hg38UCSC Ensembl
Innerchr3:3976405..4263195hg19UCSC Ensembl
Innerchr3:3951405..4238195hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38286791
hg19286791
hg18286791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4641n100
Supporting Variantsnssv3590401
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997534
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer