A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993484



Internal ID63109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15681832..15681905hg38UCSC Ensembl
chr7:15721457..15721530hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463215
Supporting Variants
Samples
Known GenesMEOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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