A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997510



Internal ID65880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52421986..52422673hg38UCSC Ensembl
chr7:52489682..52490369hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997510
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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