A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004429



Internal ID21913772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125233431..125233519hg38UCSC Ensembl
chr9:127995710..127995798hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594600
Samples
Known GenesRABEPK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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