A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477816



Internal ID22535717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24433737..24436585hg38UCSC Ensembl
chr18:22013701..22016549hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382849
hg192849
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876105
Supporting Variants
Samples
Known GenesIMPACT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477816
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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