A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027804



Internal ID19117022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143203251hg38UCSC Ensembl
Innerchr7:142827954..142900344hg19UCSC Ensembl
Innerchr7:142538076..142610466hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3872391
hg1972391
hg1872391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669642, nssv3669641
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)nsv1027804
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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