A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064169



Internal ID20631209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80969036..80969399hg38UCSC Ensembl
chr1:81434721..81435084hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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