A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766865



Internal ID19309126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132472713..132475514hg38UCSC Ensembl
chr12:133049299..133052100hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071079
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766865
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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