A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432427



Internal ID21089980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18425967..18427103hg38UCSC Ensembl
chr9:18425965..18427101hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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