A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093043



Internal ID21449578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29038667..29038667hg38UCSC Ensembl
chr16:29049988..29049988hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662040
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093043
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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