A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589508



Internal ID18887789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25235837..25285744hg38UCSC Ensembl
Innerchr3:25277328..25327235hg19UCSC Ensembl
Innerchr3:25252332..25302239hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3849908
hg1949908
hg1849908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006455
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)nssv3589508
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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