A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074852



Internal ID21477751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61179833..61179833hg38UCSC Ensembl
chr11:60947305..60947305hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648073
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074852
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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