A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745726



Internal ID21384001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6790201..7046603hg38UCSC Ensembl
chr16:6840202..7096604hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38256403
hg19256403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432357
Supporting Variants
SamplesBTQ016
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745726
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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