A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589585



Internal ID18541180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32101304..32140890hg38UCSC Ensembl
Innerchr3:32142796..32182382hg19UCSC Ensembl
Innerchr3:32117800..32157386hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3839587
hg1939587
hg1839587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003110
Supporting Variants
Samples
Known GenesGPD1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589585
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