A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060626



Internal ID20627666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26961176..26961571hg38UCSC Ensembl
chr1:27287667..27288062hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02645


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