A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142862



Internal ID20709902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33718901..33722400hg38UCSC Ensembl
chr6:33686678..33690177hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400306
Supporting Variants
Samples
Known GenesIP6K3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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