A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574120



Internal ID21522532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75248067..75248385hg38UCSC Ensembl
chr6:75957783..75958101hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146447
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574120
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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