A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025867



Internal ID19115084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99239249..99292611hg38UCSC Ensembl
Innerchr5:98574953..98628315hg19UCSC Ensembl
Innerchr5:98602853..98656215hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3853363
hg1953363
hg1853363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5723n100
Supporting Variantsnssv3640474
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)nsv1025867
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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