A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629262



Internal ID21577567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37184862..37184862hg38UCSC Ensembl
chr6:37152638..37152638hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147502
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629262
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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