A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258530



Internal ID20825570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206552812..206553152hg38UCSC Ensembl
chr2:207417536..207417876hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544664
Supporting Variants
Samples
Known GenesADAM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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