A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242190



Internal ID20809230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36507873..36562212hg38UCSC Ensembl
chr17:34863712..34918052hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3854340
hg1954341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577440
Supporting Variants
Samples
Known GenesGGNBP2, MYO19, PIGW
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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