A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434963



Internal ID21396965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3618911..3621639hg38UCSC Ensembl
chr6:3619145..3621873hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv673n172
Supporting Variantsnssv15749686
SamplesBTQ038
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434963
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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