A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589728



Internal ID18888009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42318614..42331147hg38UCSC Ensembl
Innerchr3:42360106..42372639hg19UCSC Ensembl
Innerchr3:42335110..42347643hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3812534
hg1912534
hg1812534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998682
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)nssv3589728
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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