A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109001



Internal ID20676041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121669280..121682830hg38UCSC Ensembl
chr4:122590435..122603985hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3813551
hg1913551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389671
Supporting Variants
Samples
Known GenesANXA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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