A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261628



Internal ID20828668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9513317..9513367hg38UCSC Ensembl
chr2:9653446..9653496hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542131
Supporting Variants
Samples
Known GenesADAM17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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