A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251659



Internal ID20818699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51381602..51382430hg38UCSC Ensembl
chr1:51847274..51848102hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553632
Supporting Variants
Samples
Known GenesEPS15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251659
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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