A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165270



Internal ID20732310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137450571..137450940hg38UCSC Ensembl
chr8:138462814..138463183hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165270
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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