A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937138



Internal ID22712501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9618600..9618719hg38UCSC Ensembl
chr18:9618598..9618717hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937138
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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