A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453760



Internal ID21111313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136866901..136870937hg38UCSC Ensembl
chr9:139761353..139765389hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384037
hg194037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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