A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239528



Internal ID20806568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34030075..34030459hg38UCSC Ensembl
chr15:34322276..34322660hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594553
Supporting Variants
Samples
Known GenesAVEN, CHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239528
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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