A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439434



Internal ID22105612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111414892..111414961hg38UCSC Ensembl
chr1:111957514..111957583hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758513
Samples
Known GenesOVGP1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439434
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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