A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087536



Internal ID21484112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40258882..40258882hg38UCSC Ensembl
chr15:40551083..40551083hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658552
Supporting Variants
SamplesNA12329
Known GenesPAK6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087536
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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