A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543840



Internal ID20917081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127808748..127809535hg38UCSC Ensembl
chr2:128566322..128567109hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256781
Samples
Known GenesWDR33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543840
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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