A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703620



Internal ID21375896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149327061..149327300hg38UCSC Ensembl
chr5:148706624..148706863hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392166
Supporting Variants
Samples
Known GenesAFAP1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703620
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0804598


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