A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742544



Internal ID20518528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31378215..31379077hg38UCSC Ensembl
chr10:31667144..31668006hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292182
Samples
Known GenesZEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742544
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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