A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551737



Internal ID16339146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82770450..82812197hg38UCSC Ensembl
Innerchr10:84530206..84571953hg19UCSC Ensembl
Innerchr10:84520186..84561933hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3841748
hg1941748
hg1841748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752122
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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