A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449263



Internal ID21106816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127173750..127368672hg38UCSC Ensembl
chr9:129936029..130130951hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38194923
hg19194923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219189
Samples
Known GenesGARNL3, RALGPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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