A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584831



Internal ID20957902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9453078..9454388hg38UCSC Ensembl
chr17:9356395..9357705hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243382
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584831
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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