A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256766



Internal ID20823806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127272180..127273512hg38UCSC Ensembl
chr2:128029756..128031088hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548081
Supporting Variants
Samples
Known GenesERCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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