A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265441



Internal ID20832481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95006036..95006146hg38UCSC Ensembl
chr4:95927187..95927297hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572277
Supporting Variants
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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