A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068281



Internal ID18972459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13347499..13348400hg38UCSC Ensembl
chr10:13389499..13390400hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766930
SamplesKWP1
Known GenesSEPHS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068281
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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