A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013897



Internal ID22075528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47151467..47160290hg38UCSC Ensembl
Outerchr20:47148347..47161314hg38UCSC Ensembl
Innerchr20:45780106..45788929hg19UCSC Ensembl
Outerchr20:45776986..45789953hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3812968
hg1912968
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155654
Supporting Variants
Samples
Known GenesEYA2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013897
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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