A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586101



Internal ID20959172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25738195..25739063hg38UCSC Ensembl
chr16:25749516..25750384hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38869
hg19869
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242771
Samples
Known GenesHS3ST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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