A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743675



Internal ID20519664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6404197..6404261hg38UCSC Ensembl
chr10:6446159..6446223hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743675
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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