A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609604



Internal ID21557909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3074876..3074876hg38UCSC Ensembl
chr4:3076603..3076603hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137916
SamplesHG03009
Known GenesHTT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609604
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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