A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581626



Internal ID20954697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4302261..4302827hg38UCSC Ensembl
chr16:4352262..4352828hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581626
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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