A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258156



Internal ID20825196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25583192..25583739hg38UCSC Ensembl
chr2:25806061..25806608hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539768
Supporting Variants
Samples
Known GenesDTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258156
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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