A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637054



Internal ID18935335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34051421..34187597hg38UCSC Ensembl
Innerchr5:34051526..34187702hg19UCSC Ensembl
Innerchr5:34087283..34223459hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38136177
hg19136177
hg18136177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021466
Supporting Variants
Samples
Known GenesC1QTNF3-AMACR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3637054
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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