A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948095



Internal ID22723585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87571498..87571498hg38UCSC Ensembl
chr9:90186413..90186413hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432545
Samples
Known GenesDAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948095
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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