A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634207



Internal ID21826254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21071279..21083095hg38UCSC Ensembl
chr18:18651240..18663056hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg3811817
hg1911817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038168
Supporting Variants
Samples
Known GenesROCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634207
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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