A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492004



Internal ID269229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100517442..100523134hg38UCSC Ensembl
chr10:102277199..102282891hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg385693
hg195693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038477
Samples
Known GenesSEC31B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492004
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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