A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264572



Internal ID20831612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40456898..40457248hg38UCSC Ensembl
chr4:40458915..40459265hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566137
Supporting Variants
Samples
Known GenesRBM47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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