A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147865



Internal ID21482222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21248358..21248625hg38UCSC Ensembl
chr7:21287977..21288244hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567735
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147865
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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