A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152693



Internal ID21457080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44066584..44066736hg38UCSC Ensembl
chr6:44034321..44034473hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568358
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152693
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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