A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031431



Internal ID19120653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143189898hg38UCSC Ensembl
Innerchr7:142827954..142886991hg19UCSC Ensembl
Innerchr7:142538076..142597113hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3859038
hg1959038
hg1859038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669504, nssv3759908, nssv3759909
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)nsv1031431
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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