A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251876



Internal ID20818916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45094814..45095406hg38UCSC Ensembl
chr1:45560486..45561078hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547409
Supporting Variants
Samples
Known GenesZSWIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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