A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147422



Internal ID21506498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:511284..511371hg38UCSC Ensembl
chr7:550921..551008hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570107
Supporting Variants
SamplesNA19983
Known GenesPDGFA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147422
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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