A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018177



Internal ID22079808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257353..350620hg38UCSC Ensembl
Outerchr6:254283..351304hg38UCSC Ensembl
Innerchr6:257353..350620hg19UCSC Ensembl
Outerchr6:254283..351304hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3897022
hg1997022
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156431
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018177
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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