A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558247



Internal ID21882602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103178102..103178102hg38UCSC Ensembl
chr7:102818549..102818549hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063681
Supporting Variants
Samples
Known GenesDPY19L2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558247
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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