A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447044



Internal ID21104597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118135458..118135915hg38UCSC Ensembl
chr9:120897736..120898193hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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