A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092405



Internal ID15945591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109894292..110004810hg38UCSC Ensembl
Innerchr7:109534349..109644867hg19UCSC Ensembl
Innerchr7:109321585..109432103hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38110519
hg19110519
hg18110519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608108
Supporting Variants
Samples
Known GenesEIF3IP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer