A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596303



Internal ID20969374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33127245..33127923hg38UCSC Ensembl
chr19:33618151..33618829hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245927
Samples
Known GenesGPATCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596303
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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