A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094747



Internal ID21431191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67352556..67352556hg38UCSC Ensembl
chr15:67644894..67644894hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651202
Supporting Variants
SamplesHG00731
Known GenesIQCH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094747
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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