A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533842



Internal ID18832123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23957385..24019344hg38UCSC Ensembl
Innerchr14:24426594..24488553hg19UCSC Ensembl
Innerchr14:23496434..23558393hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3861960
hg1961960
hg1861960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046815
Supporting Variants
Samples
Known GenesDHRS4, DHRS4L1, DHRS4L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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