A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567991



Internal ID21516334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3070366..3072592hg38UCSC Ensembl
chr6:3070600..3072826hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382227
hg192227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147272
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567991
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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