A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016175



Internal ID19105393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143132439..143191425hg38UCSC Ensembl
Innerchr7:142829532..142888518hg19UCSC Ensembl
Innerchr7:142539654..142598640hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3858987
hg1958987
hg1858987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669643
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)nsv1016175
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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