A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335007



Internal ID20868197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241702864..242036511hg38UCSC Ensembl
chr1:241866166..242199813hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38333648
hg19333648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200615
Samples
Known GenesEXO1, MAP1LC3C, WDR64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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