A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391252



Internal ID21382282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73417670..73418087hg38UCSC Ensembl
chr4:74283387..74283804hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703117
Samples
Known GenesALB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391252
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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