A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390965



Internal ID21382099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31203985..31204065hg38UCSC Ensembl
chr14:31673191..31673271hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705719
Samples
Known GenesHECTD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390965
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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