A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908121



Internal ID22683331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68949182..68949318hg38UCSC Ensembl
chr7:68414169..68414305hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908121
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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