A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746587



Internal ID19044868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114602745..114669440hg38UCSC Ensembl
Innerchr5:113938442..114005137hg19UCSC Ensembl
Innerchr5:113966341..114033036hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3866696
hg1966696
hg1866696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021807
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)nssv3746587
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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