A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390617



Internal ID21381752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41003396..41003533hg38UCSC Ensembl
chr13:41577532..41577669hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705555
Samples
Known GenesELF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390617
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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