A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004799



Internal ID21914142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101509526..101517909hg38UCSC Ensembl
chr10:103269283..103277666hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg388384
hg198384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583868
Samples
Known GenesBTRC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004799
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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