A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261610



Internal ID20828650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9061180..9062368hg38UCSC Ensembl
chr2:9201309..9202497hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261610
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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