A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005999



Internal ID22067630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79412948..79416990hg38UCSC Ensembl
Outerchr10:79409589..79422592hg38UCSC Ensembl
Innerchr10:81172704..81176746hg19UCSC Ensembl
Outerchr10:81169345..81182348hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3813004
hg1913004
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154630
Supporting Variants
Samples
Known GenesZCCHC24
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005999
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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