A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084137



Internal ID20651177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22570065..22570436hg38UCSC Ensembl
chr2:22792937..22793308hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00134


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