A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608109



Internal ID16395518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109902141..110002385hg38UCSC Ensembl
Innerchr7:109542198..109642442hg19UCSC Ensembl
Innerchr7:109329434..109429678hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38100245
hg19100245
hg18100245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11562n54
Supporting Variantsnssv1092406
Samples
Known GenesEIF3IP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608109
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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