A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579954



Internal ID21528439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75306792..75306841hg38UCSC Ensembl
chr6:76016508..76016557hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142726
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579954
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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