A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273998



Internal ID20841038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70435404..70436052hg38UCSC Ensembl
chr6:71145107..71145755hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555772
Supporting Variants
Samples
Known GenesFAM135A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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