A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435941



Internal ID21093494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125042353..125046332hg38UCSC Ensembl
chr9:127804632..127808611hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176648
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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