A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152329



Internal ID21412081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45770077..45770572hg38UCSC Ensembl
chr7:45809676..45810171hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567349
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152329
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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