A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444283



Internal ID21101836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127261170..127317631hg38UCSC Ensembl
chr9:130023449..130079910hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3856462
hg1956462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176794
Samples
Known GenesGARNL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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