A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381040



Internal ID22438910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40931996..40932130hg38UCSC Ensembl
chr15:41224194..41224328hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943649
Supporting Variants
Samples
Known GenesDLL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381040
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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