A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011029



Internal ID21920372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37815857..37818626hg38UCSC Ensembl
chr10:38104785..38107554hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg382770
hg192770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594187
Samples
Known GenesZNF248
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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