A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730449



Internal ID20506361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25058689..25058758hg38UCSC Ensembl
chr10:25347618..25347687hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267273
Samples
Known GenesENKUR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730449
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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