A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389287



Internal ID21380422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159096296..159098488hg38UCSC Ensembl
chr1:159066086..159068278hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704015
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389287
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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