A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444669



Internal ID21102222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131681695..131687124hg38UCSC Ensembl
chr9:134557082..134562511hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385430
hg195430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176993
Samples
Known GenesRAPGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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