A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432676



Internal ID21394678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4426279..4426529hg38UCSC Ensembl
chr18:4426279..4426529hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751696
SamplesSMI034
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432676
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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