A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1096607



Internal ID15949793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144197669..144377836hg38UCSC Ensembl
Innerchr7:143894762..144074929hg19UCSC Ensembl
Innerchr7:143525695..143705862hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38180168
hg19180168
hg18180168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608731
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1096607
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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