A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435122



Internal ID21397124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142797317..142813315hg38UCSC Ensembl
chr7:142495001..142511000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3815999
hg1916000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753009
SamplesSMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435122
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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