A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069481



Internal ID18970860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49870853..49873854hg38UCSC Ensembl
chr10:51078899..51081900hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766829
SamplesKWP1
Known GenesPARG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069481
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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