A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278633



Internal ID20845673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70630506..73057342hg38UCSC Ensembl
chr8:71542741..73969577hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg382426837
hg192426837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559446
Supporting Variants
Samples
Known GenesEYA1, KCNB2, LACTB2, LOC100132891, LOC286190, LOC392232, MSC, RNU6-83P, TERF1, TRPA1, XKR9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00043


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