A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018553



Internal ID21927896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7133239..7136131hg38UCSC Ensembl
chr10:7175201..7178093hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382893
hg192893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018553
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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