A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998107



Internal ID66284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75699833..75789513hg38UCSC Ensembl
chr7:75329151..75418831hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3889681
hg1989681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481893
Supporting Variants
Samples
Known GenesCCL26, HIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998107
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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