A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018297



Internal ID18760830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144164657..144354126hg38UCSC Ensembl
Innerchr7:143861750..144051219hg19UCSC Ensembl
Innerchr7:143492683..143682152hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38189470
hg19189470
hg18189470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6727n100
Supporting Variantsnssv3671156
Samples
Known GenesARHGEF34P, ARHGEF35, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018297
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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