A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150011



Internal ID21485500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94362621..94362621hg38UCSC Ensembl
chr5:93698326..93698326hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628633
Supporting Variants
SamplesNA12878
Known GenesKIAA0825
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150011
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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