A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737132



Internal ID20513090
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 StatusM
Merged Variants
Supporting Variantsnssv16277416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737132
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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