A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667507



Internal ID15057473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137131530..137572207hg38UCSC Ensembl
Innerchr4:138052684..138493361hg19UCSC Ensembl
Innerchr4:138272134..138712811hg18UCSC Ensembl
Innerchr4:138410289..138850966hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38440678
hg19440678
hg18440678
hg17440678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516176
Supporting Variants
Samples
Known GenesPCDH18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667507
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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