A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999932



Internal ID67534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69425692..69426352hg38UCSC Ensembl
chr7:68890678..68891338hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485015
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999932
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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