A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588018



Internal ID20961089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20193704..20348676hg38UCSC Ensembl
chr17:20097017..20251989hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38154973
hg19154973
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241505
Samples
Known GenesCCDC144CP, SPECC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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