A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608079



Internal ID16395488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109458307..110222232hg38UCSC Ensembl
Innerchr7:109098364..109862289hg19UCSC Ensembl
Innerchr7:108885600..109649525hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38763926
hg19763926
hg18763926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092086
Samples
Known GenesEIF3IP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608079
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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