A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577704



Internal ID20950775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67308301..67308864hg38UCSC Ensembl
chr16:67342204..67342767hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243606
Samples
Known GenesKCTD19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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