A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052484



Internal ID20619524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160984001..160991300hg38UCSC Ensembl
chr1:160953791..160961090hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00128


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