A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270714



Internal ID20837754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36445112..36446189hg38UCSC Ensembl
chr6:36412889..36413966hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557205
Supporting Variants
Samples
Known GenesKCTD20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270714
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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