A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610191



Internal ID21558496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120006967..120006967hg38UCSC Ensembl
chr4:120928122..120928122hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135796
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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