A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913786



Internal ID22689002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116204388..116211173hg38UCSC Ensembl
chr7:115844442..115851227hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg386786
hg196786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444366
Samples
Known GenesTES
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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