A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031198



Internal ID19120419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143125117..143191425hg38UCSC Ensembl
Innerchr7:142822210..142888518hg19UCSC Ensembl
Innerchr7:142532332..142598640hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3866309
hg1966309
hg1866309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669499, nssv3759907
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)nsv1031198
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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