A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925319



Internal ID22700546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107847479..107847535hg38UCSC Ensembl
chr7:107487924..107487980hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925319
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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