A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391681



Internal ID21382711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4756821..4756960hg38UCSC Ensembl
chr17:4660116..4660255hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706103
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391681
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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