A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870786



Internal ID22645722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19346932..19347083hg38UCSC Ensembl
chr1:19673426..19673577hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361586
Samples
Known GenesCAPZB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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