A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129286



Internal ID21410224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186433229..186433229hg38UCSC Ensembl
chr4:187354383..187354383hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640956
Supporting Variants
SamplesHG00512
Known GenesF11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129286
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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