A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589579



Internal ID18887860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28922085..28973263hg38UCSC Ensembl
Innerchr3:28963576..29014754hg19UCSC Ensembl
Innerchr3:28938580..28989758hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3851179
hg1951179
hg1851179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997877
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)nssv3589579
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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