A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3603537



Internal ID18555132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129558077..129622888hg38UCSC Ensembl
Innerchr3:129276920..129341731hg19UCSC Ensembl
Innerchr3:130759610..130824421hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3864812
hg1964812
hg1864812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014759
Supporting Variants
Samples
Known GenesPLXND1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3603537
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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