A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840236



Internal ID22615171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99149600..99151349hg38UCSC Ensembl
chr4:100070757..100072506hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498666
Samples
Known GenesLOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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