A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439879



Internal ID22106056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31713725..31714078hg38UCSC Ensembl
chr8:31571241..31571594hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758355
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439879
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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