A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243154



Internal ID20810194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61689514..61689615hg38UCSC Ensembl
chr17:59766875..59766976hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579514
Supporting Variants
Samples
Known GenesBRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243154
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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