A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656510



Internal ID21604815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79437975..79437975hg38UCSC Ensembl
chr15:79730317..79730317hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081041
SamplesHG02492
Known GenesKIAA1024
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656510
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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