A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153550



Internal ID21406620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:511336..511336hg38UCSC Ensembl
chr7:550973..550973hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633755
Supporting Variants
SamplesHG00512
Known GenesPDGFA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153550
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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