A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023470



Internal ID19112687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143191425hg38UCSC Ensembl
Innerchr7:142827954..142888518hg19UCSC Ensembl
Innerchr7:142538076..142598640hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3860565
hg1960565
hg1860565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3759913, nssv3669505, nssv3759910, nssv3669506, nssv3669507, nssv3669512, nssv3669511, nssv3669510, nssv3669509, nssv3669508, nssv3759911, nssv3759912
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)nsv1023470
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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