A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154628



Internal ID22085133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79057852..79079317hg38UCSC Ensembl
Outerchr10:79054972..79079512hg38UCSC Ensembl
Innerchr10:80817609..80839074hg19UCSC Ensembl
Outerchr10:80814729..80839269hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3824541
hg1924541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv37n97
Supporting Variantsnssv4005997
Samples
Known GenesZMIZ1, ZMIZ1-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154628
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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