A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452382



Internal ID21109935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127416554..127472639hg38UCSC Ensembl
chr9:130178833..130234918hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3856086
hg1956086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7941n223
Supporting Variantsnssv18231010
Samples
Known GenesLRSAM1, RPL12, SNORA65, ZNF79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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