A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581713



Internal ID20954784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8789435..8800912hg38UCSC Ensembl
chr17:8692753..8704230hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3811478
hg1911478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243354
Samples
Known GenesMFSD6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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