A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551568



Internal ID15992291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79068488..79070470hg38UCSC Ensembl
Innerchr10:80828245..80830227hg19UCSC Ensembl
Innerchr10:80498251..80500233hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381983
hg191983
hg181983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751748
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551568
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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