A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004420



Internal ID21913763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26186426..26427810hg38UCSC Ensembl
chr10:26475355..26716739hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38241385
hg19241385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579720
Samples
Known GenesGAD2, MYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004420
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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