A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248595



Internal ID20815635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216674616..216675323hg38UCSC Ensembl
chr1:216847958..216848665hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540110
Supporting Variants
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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