A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248775



Internal ID20815815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176141361..176141896hg38UCSC Ensembl
chr1:176110497..176111032hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547564
Supporting Variants
Samples
Known GenesRFWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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