A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155657



Internal ID22086162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60538651..60547639hg38UCSC Ensembl
Outerchr20:60535987..60553323hg38UCSC Ensembl
Innerchr20:59113709..59122697hg19UCSC Ensembl
Outerchr20:59111045..59128381hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3817337
hg1917337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013908, nssv4013909
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155657
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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