A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093642



Internal ID21492159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29063355..29063355hg38UCSC Ensembl
chr15:29355558..29355558hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654406
Supporting Variants
SamplesNA19238
Known GenesAPBA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093642
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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