A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246557



Internal ID20813597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9623544..9624420hg38UCSC Ensembl
chr19:9734220..9735096hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597153
Supporting Variants
Samples
Known GenesC19orf82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246557
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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