A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739558



Internal ID19037839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046103..4056298hg38UCSC Ensembl
Innerchr3:4087787..4097982hg19UCSC Ensembl
Innerchr3:4062787..4072982hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810196
hg1910196
hg1810196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008881
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)nssv3739558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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