A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551783



Internal ID15992506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86630480..86680809hg38UCSC Ensembl
Innerchr10:88390237..88440566hg19UCSC Ensembl
Innerchr10:88380217..88430546hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3850330
hg1950330
hg1850330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174563
SamplesNINDS_173
Known GenesLDB3, OPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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