A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026460



Internal ID19115678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29785378..29814202hg38UCSC Ensembl
Innerchr5:29785485..29814309hg19UCSC Ensembl
Innerchr5:29821242..29850066hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3828825
hg1928825
hg1828825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5615n100
Supporting Variantsnssv3636008, nssv3636010, nssv3636003, nssv3636005, nssv3636002, nssv3636007, nssv3636004, nssv3636009, nssv3636001, nssv3636006
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026460
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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