A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063880



Internal ID18806411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59844304..59922116hg38UCSC Ensembl
Innerchr20:58419359..58497171hg19UCSC Ensembl
Innerchr20:57852754..57930566hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3877813
hg1977813
hg1877813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584250, nssv3584249, nssv3584251
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)nsv1063880
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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