A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592437



Internal ID20965508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74665595..74665755hg38UCSC Ensembl
chr16:74699493..74699653hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240808
Samples
Known GenesRFWD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592437
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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