A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271889



Internal ID20838929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132165591..132167550hg38UCSC Ensembl
chr6:132486731..132488690hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565183
Supporting Variants
Samples
Known GenesLINC01013
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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