A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441246



Internal ID21098799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75087801..75089100hg38UCSC Ensembl
chr9:77702717..77704016hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224010
Samples
Known GenesNMRK1, OSTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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