A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550017



Internal ID15990740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15351310..15415762hg38UCSC Ensembl
Innerchr10:15393309..15457761hg19UCSC Ensembl
Innerchr10:15433315..15497767hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3864453
hg1964453
hg1864453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174135
Samples1780862093_A
Known GenesFAM171A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550017
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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