A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255657



Internal ID20822697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105366172..105366812hg38UCSC Ensembl
chr2:105982629..105983269hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547863
Supporting Variants
Samples
Known GenesFHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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