A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567000



Internal ID20940071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5062512..5075011hg38UCSC Ensembl
chr9:5062512..5075011hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280747
Samples
Known GenesJAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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