A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551781



Internal ID16339190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86366401..86367707hg38UCSC Ensembl
Innerchr10:88126158..88127464hg19UCSC Ensembl
Innerchr10:88116138..88117444hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381307
hg191307
hg181307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1319n54
Supporting Variantsnssv752224
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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