A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937282



Internal ID21357351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151599282..151599522hg38UCSC Ensembl
chr1:151571758..151571998hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177408
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937282
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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