A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004928



Internal ID21914271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78173130..78177058hg38UCSC Ensembl
chr10:79932887..79936815hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383929
hg193929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004928
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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