A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249644



Internal ID20816684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28098699..28099637hg38UCSC Ensembl
chr1:28425210..28426148hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249644
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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