A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447050



Internal ID21104603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79451603..79452134hg38UCSC Ensembl
chr9:82066518..82067049hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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