A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362836



Internal ID22588505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152080640..152081715hg38UCSC Ensembl
chr1:152053116..152054191hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362836
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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