A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388964



Internal ID22446834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93406699..93424745hg38UCSC Ensembl
chr15:93949928..93967974hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3818047
hg1918047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388964
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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