A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840476



Internal ID22615411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94771659..94776758hg38UCSC Ensembl
chr4:95692810..95697909hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491801
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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