A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450425



Internal ID21107978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127580585..127581392hg38UCSC Ensembl
chr9:130342864..130343671hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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