A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220139



Internal ID20787179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64992046..64992779hg38UCSC Ensembl
chr11:64759518..64760251hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586189
Supporting Variants
Samples
Known GenesBATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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