A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004185



Internal ID21913528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111555560..111555697hg38UCSC Ensembl
chr9:114317840..114317977hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591974
Samples
Known GenesPTGR1, ZNF483
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004185
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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