A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389128



Internal ID21380263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82081257..82081439hg38UCSC Ensembl
chr1:82546941..82547123hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703138
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389128
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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