A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022720



Internal ID22084351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163755234..163971936hg38UCSC Ensembl
Outerchr6:163748995..163972212hg38UCSC Ensembl
Innerchr6:164176266..164392968hg19UCSC Ensembl
Outerchr6:164170027..164393244hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38223218
hg19223218
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156608
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022720
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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