A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753009



Internal ID21392901
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 StatusS
Merged Variantsnsv4435122
Supporting Variants
SamplesSMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753009
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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