A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937359



Internal ID21357428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83692948..83693130hg38UCSC Ensembl
chr4:84614101..84614283hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195656
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937359
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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