A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575753



Internal ID20948824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23811376..23812072hg38UCSC Ensembl
chr16:23822697..23823393hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2733n223
Supporting Variantsnssv18242694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575753
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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