A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423164



Internal ID21080717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18606929..18648461hg38UCSC Ensembl
chr9:18606927..18648459hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3841533
hg1941533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221757
Samples
Known GenesADAMTSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423164
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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