A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074567



Internal ID21465895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3366380..3366380hg38UCSC Ensembl
chr11:3387610..3387610hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383049
hg193049
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651367
Supporting Variants
SamplesHG03065
Known GenesZNF195
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074567
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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