A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577504



Internal ID21525958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169142219..169142277hg38UCSC Ensembl
chr6:169542314..169542372hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152350
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577504
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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