A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874988



Internal ID22649942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23503685..23503800hg38UCSC Ensembl
chr1:23830177..23830292hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874988
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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