A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265443



Internal ID20832483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95041998..95043010hg38UCSC Ensembl
chr4:95963149..95964161hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568640
Supporting Variants
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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