A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070888



Internal ID18970217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110226441..110227442hg38UCSC Ensembl
chr10:111986199..111987200hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762423
SamplesKWP1
Known GenesMXI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070888
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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