A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582597



Internal ID21531111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5835517..5835874hg38UCSC Ensembl
chr6:5835750..5836107hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152987
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582597
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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