A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759923



Internal ID19058204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143194616hg38UCSC Ensembl
Innerchr7:142827954..142891709hg19UCSC Ensembl
Innerchr7:142538076..142601831hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3863756
hg1963756
hg1863756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020889
Supporting Variants
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)nssv3759923
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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