A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436556



Internal ID21094109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117691233..117691803hg38UCSC Ensembl
chr9:120453511..120454081hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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