A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447256



Internal ID21104809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129483666..129733968hg38UCSC Ensembl
chr9:132245945..132496247hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38250303
hg19250303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229800
Samples
Known GenesASB6, C9orf50, LINC00963, NTMT1, PRRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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