A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015769



Internal ID21925112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104132666..104133855hg38UCSC Ensembl
chr9:106894947..106896136hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588382
Samples
Known GenesSMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015769
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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