A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593561



Internal ID20966632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39895513..39895619hg38UCSC Ensembl
chr17:38051766..38051872hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593561
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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