A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426845



Internal ID21084398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1001725..1132061hg38UCSC Ensembl
chr9:1001725..1132061hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38130337
hg19130337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233882
Samples
Known GenesDMRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426845
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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