A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995027



Internal ID64111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27228613..27232532hg38UCSC Ensembl
chr7:27268232..27272151hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg383920
hg193920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995027
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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