A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002338



Internal ID21911681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33399598..33399655hg38UCSC Ensembl
chr10:33688526..33688583hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002338
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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