A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615598



Internal ID21563903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77112227..77112227hg38UCSC Ensembl
chr1:77577912..77577912hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066417
SamplesNA19239
Known GenesPIGK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615598
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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