A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193521



Internal ID20760561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6997265..7008729hg38UCSC Ensembl
chr11:7018496..7029960hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811465
hg1911465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439046
Supporting Variants
Samples
Known GenesZNF214
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193521
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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