A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023242



Internal ID19112459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143202300hg38UCSC Ensembl
Innerchr7:142827954..142899393hg19UCSC Ensembl
Innerchr7:142538076..142609515hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3871440
hg1971440
hg1871440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6698n100
Supporting Variantsnssv3669640
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)nsv1023242
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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