A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732913



Internal ID20508839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104396378..104396433hg38UCSC Ensembl
chr10:106156136..106156191hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259400
Samples
Known GenesCCDC147
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732913
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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