A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247797



Internal ID20814837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178357806..178358948hg38UCSC Ensembl
chr1:178326941..178328083hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543019
Supporting Variants
Samples
Known GenesRASAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247797
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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