A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446111



Internal ID22503981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43535921..43536212hg38UCSC Ensembl
chr6:43503658..43503949hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889709
Supporting Variants
Samples
Known GenesXPO5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446111
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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