A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364096



Internal ID22589765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177475817..177486421hg38UCSC Ensembl
chr1:177444953..177455557hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3810605
hg1910605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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