A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569637



Internal ID21517998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27190744..27192105hg38UCSC Ensembl
chr6:27158523..27159884hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153978
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569637
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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