A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006000



Internal ID22067631
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154631
Supporting Variants
Samples
Known GenesZCCHC24
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006000
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer