A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837762



Internal ID22612697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154491161..154493659hg38UCSC Ensembl
chr4:155412313..155414811hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382499
hg192499
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493532
Samples
Known GenesDCHS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837762
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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