A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539879



Internal ID20913174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178357543..178359032hg38UCSC Ensembl
chr1:178326678..178328167hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381490
hg191490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n223
Supporting Variantsnssv18248162
Samples
Known GenesRASAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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