A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238826



Internal ID20805866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64420830..64421762hg38UCSC Ensembl
chr15:64713029..64713961hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591346
Supporting Variants
Samples
Known GenesTRIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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