A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433964



Internal ID21395966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184158796..184159643hg38UCSC Ensembl
chr3:183876584..183877431hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv541n172
Supporting Variantsnssv15746253
SamplesNB10
Known GenesDVL3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433964
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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