A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005416



Internal ID21914759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77526358..77528210hg38UCSC Ensembl
chr9:80141274..80143126hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381853
hg191853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595077
Samples
Known GenesGNA14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005416
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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