A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435195



Internal ID21397197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158145309..158152308hg38UCSC Ensembl
chr7:157938001..157945000hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv789n172
Supporting Variantsnssv15752780
SamplesMDQ025
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435195
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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