A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994547



Internal ID63805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23785704..23785714hg38UCSC Ensembl
chr7:23825323..23825333hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548683
Supporting Variants
Samples
Known GenesSTK31
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994547
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002342


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