A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241594



Internal ID20808634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2600496..2600752hg38UCSC Ensembl
chr17:2503790..2504046hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591337
Supporting Variants
Samples
Known GenesPAFAH1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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