A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368870



Internal ID22594539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11020073..11075736hg38UCSC Ensembl
chr12:11172672..11228335hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855664
hg1955664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919055
Supporting Variants
Samples
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368870
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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