A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426125



Internal ID22483995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55388947..55389021hg38UCSC Ensembl
chr4:56255114..56255188hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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