A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140206



Internal ID20707246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143133401..143136400hg38UCSC Ensembl
chr6:143454538..143457537hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610744
Supporting Variants
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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