A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578069



Internal ID20951140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56410757..56411297hg38UCSC Ensembl
chr16:56444669..56445209hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239298
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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