A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929845



Internal ID21349915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108190703..108193180hg38UCSC Ensembl
chr1:108733325..108735802hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382478
hg192478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175725
SamplesHG002
Known GenesSLC25A24
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929845
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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