A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446120



Internal ID21103673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123029395..123029923hg38UCSC Ensembl
chr9:125791674..125792202hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176519
Samples
Known GenesRABGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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