A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069852



Internal ID18971247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37094498..37104099hg38UCSC Ensembl
chr15:37386699..37396300hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389602
hg199602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768611
SamplesKWP1
Known GenesMEIS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069852
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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