A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765111



Internal ID18961217
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 StatusS
Merged Variantsnsv1068691
Supporting Variants
SamplesKWP1
Known GenesPTPN20A, PTPN20B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765111
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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