A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932801



Internal ID22708105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41227538..41229214hg38UCSC Ensembl
chr15:41519736..41521412hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375738
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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