A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224979



Internal ID20792019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4124564..4794469hg38UCSC Ensembl
chr7:4164196..4834100hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38669906
hg19669905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619580
Supporting Variants
Samples
Known GenesAP5Z1, FOXK1, MIR4656, SDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224979
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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