A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247558



Internal ID20814598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16503625..16504104hg38UCSC Ensembl
chr19:16614436..16614915hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597829
Supporting Variants
Samples
Known GenesC19orf44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247558
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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