A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023679



Internal ID19112896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121354110..121554562hg38UCSC Ensembl
Innerchr5:120689805..120890257hg19UCSC Ensembl
Innerchr5:120717704..120918156hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38200453
hg19200453
hg18200453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746628
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)nsv1023679
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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