A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636535



Internal ID18934816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..157741hg38UCSC Ensembl
Innerchr5:15520..157856hg19UCSC Ensembl
Innerchr5:68520..210856hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38142222
hg19142337
hg18142337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029724
Supporting Variants
Samples
Known GenesPLEKHG4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636535
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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