A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440890



Internal ID21098443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74498301..74498900hg38UCSC Ensembl
chr9:77113217..77113816hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186409
Samples
Known GenesMIR6130, RORB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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