A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353809



Internal ID22579478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73709104..73715881hg38UCSC Ensembl
chr11:73420149..73426926hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386778
hg196778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917706
Supporting Variants
Samples
Known GenesRAB6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353809
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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