A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259280



Internal ID20826320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215840697..215841945hg38UCSC Ensembl
chr2:216705420..216706668hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540004
Supporting Variants
Samples
Known GenesLINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259280
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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