A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593166



Internal ID18891447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21942872..21981431hg38UCSC Ensembl
Innerchr3:21984364..22022923hg19UCSC Ensembl
Innerchr3:21959368..21997927hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3838560
hg1938560
hg1838560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007663
Supporting Variants
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)nssv3593166
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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