A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879851



Internal ID22654821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17358269..17358590hg38UCSC Ensembl
chr1:17684764..17685085hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352008
Samples
Known GenesPADI4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879851
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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