A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219265



Internal ID20786305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64508873..64540519hg38UCSC Ensembl
chr6:65218766..65250412hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3831647
hg1931647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399850
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219265
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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