A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590702



Internal ID20963773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7670869..7672231hg38UCSC Ensembl
chr17:7574187..7575549hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243210
Samples
Known GenesTP53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590702
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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