A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253124



Internal ID20820164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75111889..75698692hg38UCSC Ensembl
chr1:75577574..76164377hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38586804
hg19586804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541542
Supporting Variants
Samples
Known GenesLHX8, SLC44A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253124
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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