A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745967



Internal ID19044248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36448793..36461229hg38UCSC Ensembl
Innerchr5:36448895..36461331hg19UCSC Ensembl
Innerchr5:36484652..36497088hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3812437
hg1912437
hg1812437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023545
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)nssv3745967
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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