A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948391



Internal ID22723874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32472539..32472539hg38UCSC Ensembl
chr7:32512151..32512151hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948391
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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