A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739087



Internal ID20515059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74514478..74514553hg38UCSC Ensembl
chr18:72181713..72181788hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286963
Samples
Known GenesCNDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739087
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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