A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619229



Internal ID21567534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37128264..37128264hg38UCSC Ensembl
chr1:37593865..37593865hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065183, nssv17065184
SamplesHG00512, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619229
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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