A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242076



Internal ID20809116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1703323..1704178hg38UCSC Ensembl
chr17:1606617..1607472hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584251
Supporting Variants
Samples
Known GenesTLCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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