A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585181



Internal ID20958252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87539260..87541167hg38UCSC Ensembl
chr16:87572866..87574773hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381908
hg191908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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