A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002806



Internal ID21912149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103607024..103607104hg38UCSC Ensembl
chr10:105366781..105366861hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590358
Samples
Known GenesSH3PXD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002806
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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