A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251828



Internal ID20818868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44092094..44093519hg38UCSC Ensembl
chr1:44557766..44559191hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381426
hg191426
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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