A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584597



Internal ID20957668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10695462..10696845hg38UCSC Ensembl
chr17:10598779..10600162hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240967
Samples
Known GenesSCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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