A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636543



Internal ID18588138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..197317hg38UCSC Ensembl
Innerchr5:15520..197432hg19UCSC Ensembl
Innerchr5:68520..250432hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38181798
hg19181913
hg18181913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028927
Supporting Variants
Samples
Known GenesLRRC14B, PLEKHG4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636543
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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