A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261632



Internal ID20828672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9571414..9572593hg38UCSC Ensembl
chr2:9711543..9712722hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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