A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579972



Internal ID20953043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35227625..35228287hg38UCSC Ensembl
chr17:33554644..33555306hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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