A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391782



Internal ID21382812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39428040..39428156hg38UCSC Ensembl
chr17:37584293..37584409hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706160
Samples
Known GenesMED1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391782
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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