A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155393



Internal ID22085898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20527867..20701796hg38UCSC Ensembl
Outerchr17:20510133..20705288hg38UCSC Ensembl
Innerchr17:20431180..20605109hg19UCSC Ensembl
Outerchr17:20413446..20608601hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38195156
hg19195156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010176
Samples
Known GenesCDRT15L2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155393
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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