A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551573



Internal ID15992296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79068881..79070719hg38UCSC Ensembl
Innerchr10:80828638..80830476hg19UCSC Ensembl
Innerchr10:80498644..80500482hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381839
hg191839
hg181839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1274n54
Supporting Variantsnssv751754
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551573
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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