A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053402



Internal ID20620442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170490360..170492531hg38UCSC Ensembl
chr1:170459501..170461672hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382172
hg192172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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