A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994326



Internal ID63671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28431371..28436625hg38UCSC Ensembl
chr7:28470990..28476244hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg385255
hg195255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482963
Supporting Variants
Samples
Known GenesCREB5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994326
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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