A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639140



Internal ID18937421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82458452..82499864hg38UCSC Ensembl
Innerchr5:81754271..81795683hg19UCSC Ensembl
Innerchr5:81790027..81831439hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3841413
hg1941413
hg1841413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018325
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)nssv3639140
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer