A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582251



Internal ID16369660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76828757..76927389hg38UCSC Ensembl
Innerchr2:77055883..77154515hg19UCSC Ensembl
Innerchr2:76909391..77008023hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3898633
hg1998633
hg1898633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913431
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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