A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637358



Internal ID21585663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37428014..37428014hg38UCSC Ensembl
chr6:37395790..37395790hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3818444
hg1918444
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147330
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637358
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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