A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840558



Internal ID22615493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99317993..99320275hg38UCSC Ensembl
chr4:100239150..100241432hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382283
hg192283
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491848
Samples
Known GenesADH1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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