A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060785



Internal ID20627825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40943827..40947806hg38UCSC Ensembl
chr1:41409499..41413478hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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