A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364720



Internal ID22590389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14529564..14538788hg38UCSC Ensembl
chr1:14856060..14865284hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg389225
hg199225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364720
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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