A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876123



Internal ID22651083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24041293..24042068hg38UCSC Ensembl
chr1:24367783..24368558hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876123
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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