A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703309



Internal ID21375585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168881433..168881536hg38UCSC Ensembl
chr4:169802584..169802687hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391605
Supporting Variants
Samples
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703309
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0775862


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