A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487873



Internal ID265197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6824904..6833398hg38UCSC Ensembl
chr10:6866866..6875360hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg388495
hg198495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029025
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487873
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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