A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149222



Internal ID21506644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167024915..167024915hg38UCSC Ensembl
chr6:167438403..167438403hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642606
Supporting Variants
SamplesNA19983
Known GenesFGFR1OP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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