A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120672



Internal ID21511354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10631054..10631054hg38UCSC Ensembl
chr4:10632678..10632678hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386076
hg196076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608798
Supporting Variants
SamplesNA24385
Known GenesCLNK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120672
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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