A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891998



Internal ID22667042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185222031..185222109hg38UCSC Ensembl
chr4:186143185..186143263hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427513
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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