A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1096592



Internal ID15949778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144197669..144354151hg38UCSC Ensembl
Innerchr7:143894762..144051244hg19UCSC Ensembl
Innerchr7:143525695..143682177hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38156483
hg19156483
hg18156483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608725
Supporting Variants
Samples
Known GenesARHGEF34P, 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)nssv1096592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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