A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433816



Internal ID22491686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3319878..3319878hg38UCSC Ensembl
chr7:3359510..3359510hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958488
Supporting Variants
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433816
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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