A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156734



Internal ID22087135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143130861..143194628hg38UCSC Ensembl
Outerchr7:143125117..143200677hg38UCSC Ensembl
Innerchr7:142827954..142891721hg19UCSC Ensembl
Outerchr7:142822210..142897770hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3875561
hg1975561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022454
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156734
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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