A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380050



Internal ID21037603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94779016..94781794hg38UCSC Ensembl
chr4:95700167..95702945hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg382779
hg192779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120792
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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