A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478202



Internal ID255765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6836374..6861785hg38UCSC Ensembl
chr10:6878336..6903747hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3825412
hg1925412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029036
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478202
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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