A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137063



Internal ID21478637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83063272..83063802hg38UCSC Ensembl
chr4:83984425..83984955hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568936
Supporting Variants
SamplesHG03486
Known GenesCOPS4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137063
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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