A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994280



Internal ID63642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27698470..27698513hg38UCSC Ensembl
chr7:27738089..27738132hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994280
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00359


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