A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162534



Internal ID20729574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103158230..103158652hg38UCSC Ensembl
chr8:104170458..104170880hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419518
Supporting Variants
Samples
Known GenesBAALC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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