A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551692



Internal ID16339101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82016701..82050081hg38UCSC Ensembl
Innerchr10:83776457..83809837hg19UCSC Ensembl
Innerchr10:83766437..83799817hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3833381
hg1933381
hg1833381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751970
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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