A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602593



Internal ID20975664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149324101..149327100hg38UCSC Ensembl
chr6:149645237..149648236hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141863
Samples
Known GenesTAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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