A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277416



Internal ID20486634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117050801..117052338hg38UCSC Ensembl
chr1:117593423..117594960hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg381538
hg191538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277416
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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