A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068691



Internal ID18969771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46937535..47023263hg38UCSC Ensembl
chr10:46529199..46614900hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3885729
hg1985702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765111
SamplesKWP1
Known GenesPTPN20A, PTPN20B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068691
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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