A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739736



Internal ID20515711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26596368..26596450hg38UCSC Ensembl
chr1:26922859..26922941hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739736
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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