A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608237



Internal ID16048960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114614673..114650997hg38UCSC Ensembl
Innerchr7:114254728..114291052hg19UCSC Ensembl
Innerchr7:114041964..114078288hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3836325
hg1936325
hg1836325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092755
Samples
Known GenesFOXP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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