A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245220



Internal ID20812260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51234247..51234904hg38UCSC Ensembl
chr17:49311608..49312265hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578696
Supporting Variants
Samples
Known GenesMBTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245220
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00032


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