A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581064



Internal ID21529560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36710587..36710657hg38UCSC Ensembl
chr6:36678364..36678434hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145124
SamplesNA19238
Known GenesRAB44
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581064
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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