A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390771



Internal ID21381906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156786994..156787370hg38UCSC Ensembl
chr3:156504783..156505159hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707270
Samples
Known GenesLINC00886
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390771
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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