A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869935



Internal ID22644870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23890700..23891573hg38UCSC Ensembl
chr1:24217190..24218063hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360126
Samples
Known GenesCNR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869935
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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