A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420301



Internal ID21077854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17125301..17137800hg38UCSC Ensembl
chr9:17125299..17137798hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220973
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420301
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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