A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953964



Internal ID21374033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203373207..203373266hg38UCSC Ensembl
chr1:203342335..203342394hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179078
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953964
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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