A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577215



Internal ID20950286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8833564..8834175hg38UCSC Ensembl
chr17:8736881..8737492hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243356
Samples
Known GenesPIK3R6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577215
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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