A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242654



Internal ID20809694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64468589..64469079hg38UCSC Ensembl
chr17:62464706..62465196hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588908
Supporting Variants
Samples
Known GenesMILR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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