A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1097139



Internal ID15950325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144286947..144377836hg38UCSC Ensembl
Innerchr7:143984040..144074929hg19UCSC Ensembl
Innerchr7:143614973..143705862hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3890890
hg1990890
hg1890890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608854
Supporting Variants
Samples
Known GenesARHGEF5, 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)nssv1097139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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