A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982991



Internal ID21892334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241651746..241653622hg38UCSC Ensembl
chr1:241815048..241816924hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381877
hg191877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526641
Samples
Known GenesWDR64
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982991
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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