A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138653



Internal ID21405098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1026082..1026082hg38UCSC Ensembl
chr4:1019870..1019870hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607288
Supporting Variants
SamplesHG00512
Known GenesFGFRL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138653
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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