A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576820



Internal ID20949891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42066175..42066790hg38UCSC Ensembl
chr17:40218193..40218808hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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