A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551577



Internal ID16338986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79242612..79243687hg38UCSC Ensembl
Innerchr10:81002369..81003444hg19UCSC Ensembl
Innerchr10:80672375..80673450hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381076
hg191076
hg181076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1276n54
Supporting Variantsnssv751758
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551577
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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