A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444230



Internal ID21101783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121464625..121465540hg38UCSC Ensembl
chr9:124226903..124227818hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38916
hg19916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217670
Samples
Known GenesGGTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444230
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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