A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291833



Internal ID20501051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11313426..11313581hg38UCSC Ensembl
chr6:11313659..11313814hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745050
Supporting Variants
Samples
Known GenesNEDD9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291833
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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