A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551187



Internal ID15991910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63521221..63521923hg38UCSC Ensembl
Innerchr10:65280981..65281683hg19UCSC Ensembl
Innerchr10:64950987..64951689hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38703
hg19703
hg18703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748934
Samples
Known GenesREEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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