A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667386



Internal ID15057352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96735278..96870098hg38UCSC Ensembl
Innerchr5:96070982..96205801hg19UCSC Ensembl
Innerchr5:96096738..96231557hg18UCSC Ensembl
Innerchr5:96096738..96231557hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38134821
hg19134820
hg18134820
hg17134820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516293
Supporting Variants
Samples
Known GenesCAST, ERAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667386
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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