A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565041



Internal ID21889396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:511331..511383hg38UCSC Ensembl
chr7:550968..551020hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005378
Supporting Variants
Samples
Known GenesPDGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565041
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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