A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969771



Internal ID22744706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100637952..100637952hg38UCSC Ensembl
chr15:101178157..101178157hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387078
Samples
Known GenesASB7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969771
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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