A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595022



Internal ID20968093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61426419..61426804hg38UCSC Ensembl
chr17:59503780..59504165hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595022
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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