A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588047



Internal ID20961118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8224627..8224885hg38UCSC Ensembl
chr17:8127945..8128203hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243909
Samples
Known GenesCTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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