A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730291



Internal ID20506202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34275255..34275393hg38UCSC Ensembl
chr1:34740856..34740994hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730291
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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