A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016130



Internal ID19105348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143122744..143194616hg38UCSC Ensembl
Innerchr7:142819837..142891709hg19UCSC Ensembl
Innerchr7:142529959..142601831hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3871873
hg1971873
hg1871873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669496, nssv3669495, nssv3669497, nssv3669494
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016130
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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