A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872166



Internal ID22647105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203306446..203306596hg38UCSC Ensembl
chr1:203275574..203275724hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362802
Samples
Known GenesBTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872166
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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