A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073541



Internal ID21502471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130888727..130888727hg38UCSC Ensembl
chr11:130758622..130758622hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656993
Supporting Variants
SamplesNA19239
Known GenesSNX19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073541
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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