A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448078



Internal ID22114256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26372078..26372411hg38UCSC Ensembl
chr16:26383399..26383732hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759929
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448078
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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