A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608699



Internal ID16396108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144011677..144376860hg38UCSC Ensembl
Innerchr7:143708770..144073953hg19UCSC Ensembl
Innerchr7:143339703..143704886hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38365184
hg19365184
hg18365184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1096550
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A12, OR2A14, OR2A2, OR2A20P, OR2A25, OR2A42, OR2A5, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608699
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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