A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593356



Internal ID20966427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57005385..57006178hg38UCSC Ensembl
chr16:57039297..57040090hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593356
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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