A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946561



Internal ID22722053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35179934..35187870hg38UCSC Ensembl
chr18:32759898..32767834hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg387937
hg197937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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