A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217085



Internal ID20784125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149564897..149584139hg38UCSC Ensembl
chr6:149886033..149905275hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3819243
hg1919243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617755
Supporting Variants
Samples
Known GenesGINM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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