A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579845



Internal ID21528328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145300144..145301716hg38UCSC Ensembl
chr1:148255737..148257155hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg381573
hg191419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060510
SamplesHG00733
Known GenesLOC101929780, NBPF14, NBPF8, NBPF9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579845
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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