A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997618



Internal ID65957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66098062..66099872hg38UCSC Ensembl
chr7:65563049..65564859hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381811
hg191811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480970
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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