A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454169



Internal ID21111722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125224113..125226744hg38UCSC Ensembl
chr9:127986392..127989023hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176662
Samples
Known GenesRABEPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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