A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446167



Internal ID22112346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196207534..196207729hg38UCSC Ensembl
chr3:195934405..195934600hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767048
Samples
Known GenesZDHHC19
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446167
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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