A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608111



Internal ID16395520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109930700..110008155hg38UCSC Ensembl
Innerchr7:109570757..109648212hg19UCSC Ensembl
Innerchr7:109357993..109435448hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3877456
hg1977456
hg1877456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11563n54
Supporting Variantsnssv1092408
Samples
Known GenesEIF3IP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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