A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242937



Internal ID20809977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39839714..39841108hg38UCSC Ensembl
chr17:37995967..37997361hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579011
Supporting Variants
Samples
Known GenesIKZF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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