A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995501



Internal ID64440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44616699..44616710hg38UCSC Ensembl
chr7:44656298..44656309hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550237
Supporting Variants
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995501
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002185


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