A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269862



Internal ID20836902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161098252..161099893hg38UCSC Ensembl
chr6:161519284..161520925hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381642
hg191642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564274
Supporting Variants
Samples
Known GenesMAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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