A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353711



Internal ID22579380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224245679..224246758hg38UCSC Ensembl
chr1:224433381..224434460hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg381080
hg191080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872808
Supporting Variants
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353711
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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