A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581509



Internal ID20954580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45153503..45154527hg38UCSC Ensembl
chr17:43230870..43231894hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381025
hg191025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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