A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1097128



Internal ID15950314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144280907..144363467hg38UCSC Ensembl
Innerchr7:143978000..144060560hg19UCSC Ensembl
Innerchr7:143608933..143691493hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3882561
hg1982561
hg1882561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608851
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF5, 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)nssv1097128
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