A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074067



Internal ID21437941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19860082..19860082hg38UCSC Ensembl
chr11:19881628..19881628hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649761
Supporting Variants
SamplesHG00731
Known GenesNAV2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074067
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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