A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600067



Internal ID20973138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29987885..29989408hg38UCSC Ensembl
chr19:30478792..30480315hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245865
Samples
Known GenesURI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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