A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080037



Internal ID20647077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180202933..180203407hg38UCSC Ensembl
chr2:181067660..181068134hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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