A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577941



Internal ID21769984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70380137..70380294hg38UCSC Ensembl
chr11:70226243..70226400hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039409
Supporting Variants
Samples
Known GenesPPFIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577941
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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