A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154631



Internal ID22085136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79412948..79454422hg38UCSC Ensembl
Outerchr10:79409589..79455601hg38UCSC Ensembl
Innerchr10:81172704..81214178hg19UCSC Ensembl
Outerchr10:81169345..81215357hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3846013
hg1946013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006000
Samples
Known GenesZCCHC24
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154631
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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