A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972784



Internal ID22747719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88086518..88086518hg38UCSC Ensembl
chr15:88629749..88629749hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382866
Samples
Known GenesNTRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972784
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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