A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446778



Internal ID21104331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127499479..127500358hg38UCSC Ensembl
chr9:130261758..130262637hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176806
Samples
Known GenesLRSAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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