A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952007



Internal ID22727342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109337068..109337068hg38UCSC Ensembl
chr8:110349297..110349297hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436573
Samples
Known GenesENY2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952007
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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