A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698953



Internal ID21220803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167940335..167940564hg38UCSC Ensembl
chr6:168341015..168341244hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813992
Supporting Variants
Samples
Known GenesMLLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698953
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.741379


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