A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391280



Internal ID21382310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41206176..41206272hg38UCSC Ensembl
chr15:41498374..41498470hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705880
Samples
Known GenesEXD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391280
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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