A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426676



Internal ID22484546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149327060..149327299hg38UCSC Ensembl
chr5:148706623..148706862hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906908
Supporting Variants
Samples
Known GenesAFAP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426676
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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