A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609342



Internal ID21557647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154924418..154924418hg38UCSC Ensembl
chr4:155845570..155845570hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123608
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609342
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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