A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434726



Internal ID21396728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111320039..111321960hg38UCSC Ensembl
chr6:111641242..111643163hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381922
hg191922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv712n172
Supporting Variantsnssv15753095
SamplesMDQ045
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434726
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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