A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901898



Internal ID22677051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112726098..112726213hg38UCSC Ensembl
chr5:112061795..112061910hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428922
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901898
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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