A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577964



Internal ID20951035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49637346..49638627hg38UCSC Ensembl
chr17:47714708..47715989hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381282
hg191282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245144
Samples
Known GenesSPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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