A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585590



Internal ID18883871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207476490..207493551hg38UCSC Ensembl
Innerchr2:208341214..208358275hg19UCSC Ensembl
Innerchr2:208049459..208066520hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3817062
hg1917062
hg1817062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008613
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)nssv3585590
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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