A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241542



Internal ID20808582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21187643..21188135hg38UCSC Ensembl
chr17:21090956..21091448hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578618
Supporting Variants
Samples
Known GenesDHRS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241542
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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