A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246302



Internal ID20813342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42046929..42047131hg38UCSC Ensembl
chr19:42551081..42551283hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596166
Supporting Variants
Samples
Known GenesGRIK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246302
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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