A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053618



Internal ID20620658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168646333..168646564hg38UCSC Ensembl
chr1:168615571..168615802hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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