A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019742



Internal ID21929085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3643378..3643434hg38UCSC Ensembl
chr7:3683010..3683066hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565694
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019742
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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