A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639186



Internal ID18937467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:89913895..89941143hg38UCSC Ensembl
Innerchr5:89209712..89236960hg19UCSC Ensembl
Innerchr5:89245468..89272716hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3827249
hg1927249
hg1827249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029821
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)nssv3639186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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