A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608854



Internal ID16396263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144286947..144377836hg38UCSC Ensembl
Innerchr7:143984040..144074929hg19UCSC Ensembl
Innerchr7:143614973..143705862hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3890890
hg1990890
hg1890890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11685n54
Supporting Variantsnssv1097139
Samples
Known GenesARHGEF5, OR2A1, OR2A20P, OR2A42, OR2A9P, RNU6-57P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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