A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507095



Internal ID283824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118358530..118358600hg38UCSC Ensembl
chr10:120118042..120118112hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040797
Samples
Known GenesLINC00867
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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