A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618780



Internal ID21810827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21592346..21592525hg38UCSC Ensembl
chr18:19172307..19172486hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035139
Supporting Variants
Samples
Known GenesESCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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