A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448976



Internal ID22115154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269668..77269733hg38UCSC Ensembl
chr14:77736011..77736076hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756479
Samples
Known GenesNGB
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448976
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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