A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639942



Internal ID18591537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96746697..97036461hg38UCSC Ensembl
Innerchr5:96082401..96372165hg19UCSC Ensembl
Innerchr5:96108157..96397921hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38289765
hg19289765
hg18289765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028741
Supporting Variants
Samples
Known GenesCAST, ERAP1, ERAP2, LNPEP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639942
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer