A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895204



Internal ID22670283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11313405..11313559hg38UCSC Ensembl
chr6:11313638..11313792hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420163
Samples
Known GenesNEDD9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895204
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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