A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449615



Internal ID21107168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131718401..131727900hg38UCSC Ensembl
chr9:134593788..134603287hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176994
Samples
Known GenesRAPGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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