A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242595



Internal ID20809635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6267389..6288718hg38UCSC Ensembl
chr17:6170709..6192038hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3821330
hg1921330
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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