A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608231



Internal ID16048954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114067732..114419101hg38UCSC Ensembl
Innerchr7:113707787..114059156hg19UCSC Ensembl
Innerchr7:113495023..113846392hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38351370
hg19351370
hg18351370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092751
Samples
Known GenesFOXP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608231
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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