A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438462



Internal ID21096015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118323219..118323574hg38UCSC Ensembl
chr9:121085497..121085852hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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