A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892205



Internal ID22667251
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 StatusM
Merged Variants
Supporting Variantsnssv17425371
Samples
Known GenesCOPS4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892205
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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