A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837401



Internal ID22612336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140321583..140326082hg38UCSC Ensembl
chr4:141242737..141247236hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492930
Samples
Known GenesLOC100129858, SCOC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837401
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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