A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220775



Internal ID20787815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13930573..13931034hg38UCSC Ensembl
chr7:13970198..13970659hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602702
Supporting Variants
Samples
Known GenesETV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220775
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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