A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742968



Internal ID20518954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114583451..114583505hg38UCSC Ensembl
chr10:116343210..116343264hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276214
Samples
Known GenesABLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742968
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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