A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549975



Internal ID15990698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12561913..12622575hg38UCSC Ensembl
Innerchr10:12603912..12664574hg19UCSC Ensembl
Innerchr10:12643918..12704580hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860663
hg1960663
hg1860663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174124
SamplesHGDP00057
Known GenesCAMK1D, MIR4480
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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