A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976501



Internal ID22751436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65269185..65269185hg38UCSC Ensembl
chr15:65561523..65561523hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374832
Samples
Known GenesPARP16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976501
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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