A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221917



Internal ID20788957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66946768..67436672hg38UCSC Ensembl
chr7:66411755..66901659hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38489905
hg19489905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617096
Supporting Variants
Samples
Known GenesLOC101929736, MIR4650-1, MIR4650-2, PMS2P4, SBDS, STAG3L4, TMEM248, TYW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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