A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585356



Internal ID16372765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7404601..7419548hg38UCSC Ensembl
Innerchr20:7385248..7400195hg19UCSC Ensembl
Innerchr20:7333248..7348195hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3814948
hg1914948
hg1814948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7453n54
Supporting Variantsnssv937575
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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