A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026139



Internal ID19115356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143200665hg38UCSC Ensembl
Innerchr7:142827954..142897758hg19UCSC Ensembl
Innerchr7:142538076..142607880hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3869805
hg1969805
hg1869805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669639, nssv3759973, nssv3669638, nssv3759976, nssv3759977, nssv3669635, nssv3669633, nssv3669634, nssv3759978, nssv3759975, nssv3669631, nssv3669632, nssv3669637, nssv3759974, nssv3669636
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)nsv1026139
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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