A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050913



Internal ID20617953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111601164..111601775hg38UCSC Ensembl
chr1:112143786..112144397hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333595
Supporting Variants
Samples
Known GenesLOC100129269
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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