A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075544



Internal ID21498269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59554887..59554887hg38UCSC Ensembl
chr11:59322360..59322360hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647722
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075544
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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