A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068675



Internal ID18976378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15168400..15169101hg38UCSC Ensembl
chr10:15210399..15211100hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772974
SamplesKWP1
Known GenesNMT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068675
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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