A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009816



Internal ID21919159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75750612..75750692hg38UCSC Ensembl
chr10:77510370..77510450hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009816
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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