A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663625



Internal ID21611930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90499338..90499338hg38UCSC Ensembl
chr15:91042570..91042570hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084070
SamplesHG01114
Known GenesIQGAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663625
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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