A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119725



Internal ID20686765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92636417..92820757hg38UCSC Ensembl
chr4:93557568..93741908hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38184341
hg19184341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380821
Supporting Variants
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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