A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009103



Internal ID21918446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127176945..127189931hg38UCSC Ensembl
chr9:129939224..129952210hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3812987
hg1912987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578945
Samples
Known GenesRALGPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009103
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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