A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376882



Internal ID22434752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32176882..32176949hg38UCSC Ensembl
chr18:29756845..29756912hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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