A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122539



Internal ID20689579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90043287..90340633hg38UCSC Ensembl
chr4:90964438..91261784hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38297347
hg19297347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382555
Supporting Variants
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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