A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373272



Internal ID22598941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40344937..40345029hg38UCSC Ensembl
chr15:40637138..40637230hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373272
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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