A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435156



Internal ID21397158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155345301..155349297hg38UCSC Ensembl
chr7:155138001..155142000hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383997
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754451
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435156
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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