A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946407



Internal ID21366477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165761972..165762252hg38UCSC Ensembl
chr1:165731209..165731489hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176905
SamplesHG002
Known GenesTMCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946407
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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