A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058471



Internal ID19147690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39060545..39084842hg38UCSC Ensembl
Innerchr20:37689188..37713485hg19UCSC Ensembl
Innerchr20:37122602..37146899hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3824298
hg1924298
hg1824298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584777
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)nsv1058471
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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