A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057535



Internal ID20624575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216713832..216714274hg38UCSC Ensembl
chr1:216887174..216887616hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326474
Supporting Variants
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057535
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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