A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436286



Internal ID21093839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74383958..74384513hg38UCSC Ensembl
chr9:76998874..76999429hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184000
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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