A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022192



Internal ID19111410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18565136..18830479hg38UCSC Ensembl
Innerchr5:18565245..18830588hg19UCSC Ensembl
Innerchr5:18601002..18866345hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38265344
hg19265344
hg18265344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635857
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)nsv1022192
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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