A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444002



Internal ID21101555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124918513..124920684hg38UCSC Ensembl
chr9:127680792..127682963hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382172
hg192172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226868
Samples
Known GenesGOLGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444002
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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