A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608236



Internal ID16048959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114446139..114505251hg38UCSC Ensembl
Innerchr7:114086194..114145306hg19UCSC Ensembl
Innerchr7:113873430..113932542hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3859113
hg1959113
hg1859113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11584n54
Supporting Variantsnssv1155388
SamplesHGDP00043
Known GenesFOXP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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