A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551571



Internal ID15992294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79068826..79070719hg38UCSC Ensembl
Innerchr10:80828583..80830476hg19UCSC Ensembl
Innerchr10:80498589..80500482hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381894
hg191894
hg181894
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751751, nssv751752
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551571
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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