A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073874



Internal ID21472944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23672550..23672550hg38UCSC Ensembl
chr11:23694096..23694096hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652769
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073874
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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