A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951727



Internal ID22727080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112717908..112717908hg38UCSC Ensembl
chr5:112053605..112053605hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427556
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951727
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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