A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589662



Internal ID18887943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36590547..36615998hg38UCSC Ensembl
Innerchr3:36632039..36657490hg19UCSC Ensembl
Innerchr3:36607043..36632494hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3825452
hg1925452
hg1825452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002734
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)nssv3589662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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