A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242593



Internal ID20809633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62638906..62639902hg38UCSC Ensembl
chr17:60716267..60717263hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590160
Supporting Variants
Samples
Known GenesMRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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