A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018996



Internal ID19108213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143125117..143200665hg38UCSC Ensembl
Innerchr7:142822210..142897758hg19UCSC Ensembl
Innerchr7:142532332..142607880hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3875549
hg1975549
hg1875549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669501, nssv3669502, nssv3669500
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)nsv1018996
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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