A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590104



Internal ID20963175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42320635..42321381hg38UCSC Ensembl
chr17:40472653..40473399hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242995
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590104
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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