A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443580



Internal ID22109763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84650274..84653634hg38UCSC Ensembl
chr3:84699425..84702785hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg383361
hg193361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761486
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443580
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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