A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747934



Internal ID20523957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137538118..137538209hg38UCSC Ensembl
chr4:138459272..138459363hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747934
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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