A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537678



Internal ID312919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6894540..6894551hg38UCSC Ensembl
chr10:6936502..6936513hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537678
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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