A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616614



Internal ID21564919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7903135..7903135hg38UCSC Ensembl
chr1:7963195..7963195hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066128
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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