A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585358



Internal ID16372767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7408420..7422657hg38UCSC Ensembl
Innerchr20:7389067..7403304hg19UCSC Ensembl
Innerchr20:7337067..7351304hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3814238
hg1914238
hg1814238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7453n54
Supporting Variantsnssv937578, nssv937577
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585358
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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