A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153286



Internal ID21508119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:153815221..153816719hg38UCSC Ensembl
chr7:153512306..153513804hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579075
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153286
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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