A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477851



Internal ID22535752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28993365..29011313hg38UCSC Ensembl
chr18:26573329..26591277hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3817949
hg1917949
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477851
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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