A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391429



Internal ID21382459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121055497..121055648hg38UCSC Ensembl
chr4:121976652..121976803hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703213
Samples
Known GenesNDNF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391429
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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