A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227992



Internal ID20795032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50049509..50255036hg38UCSC Ensembl
chr10:51809269..52014796hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38205528
hg19205528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589619
Supporting Variants
Samples
Known GenesASAH2, FAM21A, FAM21B, FLJ31813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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