A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440818



Internal ID22106996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34817161..34817212hg38UCSC Ensembl
chr20:33404964..33405015hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763834
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440818
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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