A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589561



Internal ID18887842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26569994..26580932hg38UCSC Ensembl
Innerchr3:26611485..26622423hg19UCSC Ensembl
Innerchr3:26586489..26597427hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3810939
hg1910939
hg1810939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999220
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)nssv3589561
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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