A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073643



Internal ID19318326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52409983..52410684hg38UCSC Ensembl
chr3:52443999..52444700hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772859
SamplesKWP1
Known GenesBAP1, PHF7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073643
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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