A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061554



Internal ID20628594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46324673..46331034hg38UCSC Ensembl
chr1:46790345..46796706hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg386362
hg196362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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