A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751766



Internal ID15699036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79242718..79243739hg38UCSC Ensembl
Innerchr10:81002475..81003496hg19UCSC Ensembl
Innerchr10:80672481..80673502hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381022
hg191022
hg181022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551583
Supporting Variants
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751766
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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