A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759974



Internal ID19058255
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 StatusS
Merged Variantsnsv1026139
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)nssv3759974
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer