A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573650



Internal ID20946721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75073719..75074154hg38UCSC Ensembl
chr9:77688635..77689070hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280988
Samples
Known GenesNMRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573650
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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