A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746559



Internal ID19044840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110108905..110150741hg38UCSC Ensembl
Innerchr5:109444606..109486442hg19UCSC Ensembl
Innerchr5:109472505..109514341hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3841837
hg1941837
hg1841837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015369
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)nssv3746559
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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