A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087352



Internal ID21491255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90008426..90008426hg38UCSC Ensembl
chr15:90551658..90551658hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657069
Supporting Variants
SamplesNA19238
Known GenesZNF710
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087352
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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