A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559007



Internal ID20932078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74431764..74431868hg38UCSC Ensembl
chr9:77046680..77046784hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280962
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559007
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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