A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447904



Internal ID21105457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71869788..71922689hg38UCSC Ensembl
chr9:74484704..74537605hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3852902
hg1952902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223470
Samples
Known GenesABHD17B, C9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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