A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051151



Internal ID20618191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109101414..109102042hg38UCSC Ensembl
chr1:109644036..109644664hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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