A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069516



Internal ID18977994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114043640..114044241hg38UCSC Ensembl
chr10:115803399..115804000hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764375
SamplesKWP1
Known GenesADRB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069516
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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