A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284018



Internal ID20493236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109030608..109032557hg38UCSC Ensembl
chr1:109573230..109575179hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381950
hg191950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733174
Supporting Variants
Samples
Known GenesWDR47
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284018
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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