A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565407



Internal ID21757953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4020468..4416545hg38UCSC Ensembl
chr7:4060100..4456176hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38396078
hg19396077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004347
Supporting Variants
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565407
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer