A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445860



Internal ID21103413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128768721..128769189hg38UCSC Ensembl
chr9:131531000..131531468hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176909
Samples
Known GenesZER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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