A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432356



Internal ID21394358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6790200..7046799hg38UCSC Ensembl
chr16:6840201..7096800hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38256600
hg19256600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv278n172
Supporting Variantsnssv15747599, nssv15749165, nssv15745829
SamplesSMI034, BTQ038, SMI041
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432356
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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