A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055705



Internal ID18798236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59845169..59922116hg38UCSC Ensembl
Innerchr20:58420224..58497171hg19UCSC Ensembl
Innerchr20:57853619..57930566hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3876948
hg1976948
hg1876948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584256, nssv3584255
Samples
Known GenesPHACTR3, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055705
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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