A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479911



Internal ID22537813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80106891..80112419hg38UCSC Ensembl
chr18:77864775..77870302hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg385529
hg195528
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882591
Supporting Variants
Samples
Known GenesADNP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479911
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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