A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954605



Internal ID22729840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22851817..22851817hg38UCSC Ensembl
chr7:22891436..22891436hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954605
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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