A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764167



Internal ID18958263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18280993..18281053hg38UCSC Ensembl
chr10:18569922..18569982hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069459
Supporting Variants
SamplesKWP1
Known GenesCACNB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764167
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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