A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937832



Internal ID22713205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38718683..38718948hg38UCSC Ensembl
chr18:36298647..36298912hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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