A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061135



Internal ID20628175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46230861..46233062hg38UCSC Ensembl
chr1:46696533..46698734hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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