A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598461



Internal ID20971532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55090504..55214873hg38UCSC Ensembl
chr19:55601872..55726241hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38124370
hg19124370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248480
Samples
Known GenesDNAAF3, PPP1R12C, PTPRH, SYT5, TNNI3, TNNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598461
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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