A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581025



Internal ID20954096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61500348..61514380hg38UCSC Ensembl
chr16:61534252..61548284hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3814033
hg1914033
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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