A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432657



Internal ID21394659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37565711..37567421hg38UCSC Ensembl
chr18:35145674..35147384hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754542
SamplesMDQ025
Known GenesCELF4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432657
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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