A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058288



Internal ID20625328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224713366..224714611hg38UCSC Ensembl
chr1:224901068..224902313hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334146
Supporting Variants
Samples
Known GenesCNIH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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