A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258609



Internal ID20825649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210084168..210084650hg38UCSC Ensembl
chr2:210948892..210949374hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553986
Supporting Variants
Samples
Known GenesKANSL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258609
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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