A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006397



Internal ID21915740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125227469..125227556hg38UCSC Ensembl
chr9:127989748..127989835hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597393
Samples
Known GenesRABEPK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006397
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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