A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918141



Internal ID22693362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76319784..76320669hg38UCSC Ensembl
chr7:75949101..75949986hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1908n209
Supporting Variantsnssv17446135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918141
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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