A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929156



Internal ID22704405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3740796..3740885hg38UCSC Ensembl
chr18:3740796..3740885hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376573
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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