A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874412



Internal ID22649364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44997589..44998322hg38UCSC Ensembl
chr1:45463261..45463994hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874412
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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