A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746583



Internal ID19044864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114082815..114157254hg38UCSC Ensembl
Innerchr5:113418512..113492951hg19UCSC Ensembl
Innerchr5:113446411..113520850hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3874440
hg1974440
hg1874440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020064
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)nssv3746583
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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