A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368665



Internal ID21026218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16723439..16724053hg38UCSC Ensembl
chr4:16725062..16725676hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112504
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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