A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055397



Internal ID20622437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188662441..188663154hg38UCSC Ensembl
chr1:188631572..188632285hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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