A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967605



Internal ID22742540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74871314..74871314hg38UCSC Ensembl
chr15:75163655..75163655hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372220
Samples
Known GenesSCAMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967605
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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