A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434070



Internal ID21396072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56697805..56698874hg38UCSC Ensembl
chr3:56731833..56732902hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749201
SamplesBTQ038
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434070
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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