A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148318



Internal ID21508638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22510291..22512062hg38UCSC Ensembl
chr7:22549910..22551681hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381772
hg191772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577174
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148318
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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