A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005997



Internal ID22067628
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 Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154628
Supporting Variants
Samples
Known GenesZMIZ1, ZMIZ1-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005997
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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