A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070097



Internal ID19317162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19168515..19168580hg38UCSC Ensembl
chr12:19321449..19321514hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764680
SamplesKWP1
Known GenesPLEKHA5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070097
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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