A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593384



Internal ID18891665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:55919405..55966599hg38UCSC Ensembl
Innerchr3:55953433..56000627hg19UCSC Ensembl
Innerchr3:55928473..55975667hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3847195
hg1947195
hg1847195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999867
Supporting Variants
Samples
Known GenesERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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