A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148313



Internal ID21505304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:510628..510798hg38UCSC Ensembl
chr7:550265..550435hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567403
Supporting Variants
SamplesNA19650
Known GenesPDGFA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148313
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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