A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617694



Internal ID21565999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60678907..60678907hg38UCSC Ensembl
chr1:61144579..61144579hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065687
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617694
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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