A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058684



Internal ID18801215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39055259..40107402hg38UCSC Ensembl
Innerchr20:37683902..38736043hg19UCSC Ensembl
Innerchr20:37117316..38169457hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381052144
hg191052142
hg181052142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584776
Samples
Known GenesLOC339568
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058684
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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