A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000565



Internal ID67955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103178051..103178075hg38UCSC Ensembl
chr7:102818498..102818522hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547177
Supporting Variants
Samples
Known GenesDPY19L2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000565
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.113487


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