A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551809



Internal ID16339218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942633..86943239hg38UCSC Ensembl
Innerchr10:88702390..88702996hg19UCSC Ensembl
Innerchr10:88692370..88692976hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38607
hg19607
hg18607
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1326n54
Supporting Variantsnssv752257, nssv752256
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551809
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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