A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242622



Internal ID20809662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63729514..63729860hg38UCSC Ensembl
chr17:61806874..61807220hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584906
Supporting Variants
Samples
Known GenesSTRADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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