A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565409



Internal ID21513721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1897923..1898046hg38UCSC Ensembl
chr6:1898157..1898280hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145419
SamplesHG03065
Known GenesGMDS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565409
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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