A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157690



Internal ID21441261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73563565..73563672hg38UCSC Ensembl
chr6:74273288..74273395hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565673
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157690
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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