A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490256



Internal ID267515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59745529..59745632hg38UCSC Ensembl
chr10:61505287..61505390hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035851
Samples
Known GenesLINC00948
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490256
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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