A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019647



Internal ID21928990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92556650..92556817hg38UCSC Ensembl
chr10:94316407..94316574hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593946
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019647
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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