A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736332



Internal ID20512280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9877537..9877907hg38UCSC Ensembl
chr18:9877534..9877904hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736332
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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