A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551798



Internal ID16339207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942473..86943081hg38UCSC Ensembl
Innerchr10:88702230..88702838hg19UCSC Ensembl
Innerchr10:88692210..88692818hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38609
hg19609
hg18609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1325n54
Supporting Variantsnssv752239
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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