A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056405



Internal ID18798936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38279584..38343306hg38UCSC Ensembl
Innerchr20:36907986..36971709hg19UCSC Ensembl
Innerchr20:36341400..36405123hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3863723
hg1963724
hg1863724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4309n100
Supporting Variantsnssv3584774
Samples
Known GenesBPI, LOC149684
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056405
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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